SPONGIT: Comparison of Two Surgical Approaches in the Treatment of Degenerative Spondylolysthesis

NCT ID: NCT00869882

Last Updated: 2014-10-30

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2009-06-30

Study Completion Date

2013-11-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

This trial, conducted in adult patients with degenerative spondylolisthesis needing surgical treatment at one level, aimed at comparing two approaches of spinal fusion.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Degenerative spondylolisthesis is defined as the slip of one vertebra onto the other due to degenerative lesions; the L4-L5 intervertebral space is mainly involved. Mean age of symptomatic disease is about 60. Surgery is indicated in the presence of radiculalgia and/or neurological claudication and/or invalidating lombalgia, worsening neurological deficit, presence of sphincterian incontinence.

Surgical treatment of degenerative spondylolisthesis usually consists in neural decompression followed by posterolateral fusion with instrumentation. In the literature, fusion rate is estimated to be 80% with GPLI and seems to be increased by interbody fusion, especially transforaminal lumbar interbody fusion which has the advantage of unilateral disc interspace route, and fusion rate over 90%.

It seems that hypolordosis in the instrumented segments caused increased loading of the posterior column in the adjacent segments. These biomechanical effects may explain the degenerative changes at the junction level that have been observed as long-term consequences of lumbar fusion.

In addition to fusion, segmental lordosis gain seems to be an important long-term prognostic factor. Segmental lordosis recovery (upper than 3° in order to take into account measurement variability), was never assessed after TLIF procedure nor compared to that after posterolateral fusion in controlled randomized clinical trials.

The main objective of the study is the comparison of efficacy between circumferential fusion (TLIF plus GPLI) and GPLI alone as surgical treatment of degenerative spondylolisthesis in term of "Success" rate, defined as fusion and at least 3-degree increase of segmental lordosis angle, 24 months after surgery.

In this trial, included patients will be randomly assigned to undergo either posterolateral fusion with instrumentation (GPLI) or circumferential fusion with transforaminal lumbar interbody fusion (TLIF) combined to GPLI. In both arms, bone autograft will be performed using loose fragments obtained during neurological decompression.

Six visits are planned during the study: pre-inclusion visit within 3 months before surgery, inclusion/randomisation on the day before surgery, 3 follow-up visits (2, 6, and 12 months after surgery) and an end of study visit 24 months after surgery (or at time of withdrawal if relevant). Hospital stay (about one week, on average) is planned after surgery.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Degenerative Spondylolisthesis

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

1

Posterolateral fusion with instrumentation combined to transforaminal lumbar interbody fusion

Group Type EXPERIMENTAL

Circumferential arthrodesis

Intervention Type PROCEDURE

Patients are carefully positioned in the proned position and submitted to a posterior surgical approach under general anaesthesia. Surgical levels are viewed laterally by mean of intraoperative radiographs which can be performed at surgeon's demand during the whole surgery time.

The preceding procedure is performed. In case of foraminal stenosis, decompression is performed at the same time as discal approach via the narrowest foramen.

In addition to this, before preparation of bed for bone grafting, nerve roots are retracted and the disc nucleus is removed entirely, then endplate decortication is performed. The disc space is distracted. The most anterior part of the disc space is packed with cancellous bone. A cage packed with bone is inserted into the anterior portion of the interspace. According to cage location, bone graft could be inserted in the posterior portion of the interspace. Cage placement is radiologically checked.

The end of the procedure is the same as for GPLI.

2

Posterolateral fusion with instrumentation

Group Type ACTIVE_COMPARATOR

Posterolateral fusion with instrumentation

Intervention Type PROCEDURE

Patients are carefully positioned in pronation and submitted to a posterior surgical approach under general anaesthesia. Surgical levels are viewed laterally by mean of intraoperative radiographs performed at surgeon's demand during the whole surgery time.

Pedicle screw instrumentation is performed, followed by posterior neural decompression depending on the type of stenosis:

* Central stenosis: decompression is performed including medial facectomy, laminectomy;
* Foraminal stenosis: foraminotomy is performed, while preserving a graft bed as large as possible;
* Pure foraminal stenosis: spinal duct is not opened. Local bone is harvested from the lamina and the spinous process and carefully fragmented for autologous graft.

Subperiosteal dissection is performed between the transverse processes and lateral aspects of the facet joints.

Two rods are placed and locked on screws in maximum compression to optimize segmental lordosis.

Bone autograft is placed into this bed.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Circumferential arthrodesis

Patients are carefully positioned in the proned position and submitted to a posterior surgical approach under general anaesthesia. Surgical levels are viewed laterally by mean of intraoperative radiographs which can be performed at surgeon's demand during the whole surgery time.

The preceding procedure is performed. In case of foraminal stenosis, decompression is performed at the same time as discal approach via the narrowest foramen.

In addition to this, before preparation of bed for bone grafting, nerve roots are retracted and the disc nucleus is removed entirely, then endplate decortication is performed. The disc space is distracted. The most anterior part of the disc space is packed with cancellous bone. A cage packed with bone is inserted into the anterior portion of the interspace. According to cage location, bone graft could be inserted in the posterior portion of the interspace. Cage placement is radiologically checked.

The end of the procedure is the same as for GPLI.

Intervention Type PROCEDURE

Posterolateral fusion with instrumentation

Patients are carefully positioned in pronation and submitted to a posterior surgical approach under general anaesthesia. Surgical levels are viewed laterally by mean of intraoperative radiographs performed at surgeon's demand during the whole surgery time.

Pedicle screw instrumentation is performed, followed by posterior neural decompression depending on the type of stenosis:

* Central stenosis: decompression is performed including medial facectomy, laminectomy;
* Foraminal stenosis: foraminotomy is performed, while preserving a graft bed as large as possible;
* Pure foraminal stenosis: spinal duct is not opened. Local bone is harvested from the lamina and the spinous process and carefully fragmented for autologous graft.

Subperiosteal dissection is performed between the transverse processes and lateral aspects of the facet joints.

Two rods are placed and locked on screws in maximum compression to optimize segmental lordosis.

Bone autograft is placed into this bed.

Intervention Type PROCEDURE

Other Intervention Names

Discover alternative or legacy names that may be used to describe the listed interventions across different sources.

TLIF+GPLI GPLI

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Adults aged less than 75,
* Having been informed about clinical trial objectives and risk,
* Covered by health insurance system,
* Suffering from degenerative spondylolisthesis (whatever the grade and intervertebral disc height) needing one-level surgical fusion due to either invalidating lombalgia/radiculalgia despite 6-month optimal medical treatment and/or motor neurological symptoms.

Exclusion Criteria

* Previous lumbar fusion,
* Previous spine traumatism,
* Presence of at least one major contraindication to surgery and/or general anaesthesia (ie, non controlled coagulopathy, active infection, or serious underlying disease, auto-immune affection).
* Presence of at least one contraindication to either TLIF or GPLI,
* Severe radiological osteoporosis.
* Active cancer at time of inclusion into the study.
* Unlikely to comply with the requirements of the study and/or to complete the study for psychological, social, familial or geographical reasons.
* Under any administrative or legal supervision.
Minimum Eligible Age

18 Years

Maximum Eligible Age

74 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

University Hospital, Bordeaux

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Patrick GUERIN, MD

Role: PRINCIPAL_INVESTIGATOR

University Hospital Bordeaux, France

Antoine BENARD, MD

Role: STUDY_CHAIR

University Hospital Bordeaux, France

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Service de chirurgie orthopédique, Hôpital Pellegrin Tripode

Bordeaux, , France

Site Status

Countries

Review the countries where the study has at least one active or historical site.

France

References

Explore related publications, articles, or registry entries linked to this study.

Rosenberg NJ. Degenerative spondylolisthesis. Predisposing factors. J Bone Joint Surg Am. 1975 Jun;57(4):467-74.

Reference Type BACKGROUND
PMID: 1141255 (View on PubMed)

Frymoyer JW. Degenerative Spondylolisthesis: Diagnosis and Treatment. J Am Acad Orthop Surg. 1994 Jan;2(1):9-15. doi: 10.5435/00124635-199401000-00002.

Reference Type BACKGROUND
PMID: 10708989 (View on PubMed)

Cummins J, Lurie JD, Tosteson TD, Hanscom B, Abdu WA, Birkmeyer NJ, Herkowitz H, Weinstein J. Descriptive epidemiology and prior healthcare utilization of patients in the Spine Patient Outcomes Research Trial's (SPORT) three observational cohorts: disc herniation, spinal stenosis, and degenerative spondylolisthesis. Spine (Phila Pa 1976). 2006 Apr 1;31(7):806-14. doi: 10.1097/01.brs.0000207473.09030.0d.

Reference Type BACKGROUND
PMID: 16582855 (View on PubMed)

Taylor VM, Deyo RA, Cherkin DC, Kreuter W. Low back pain hospitalization. Recent United States trends and regional variations. Spine (Phila Pa 1976). 1994 Jun 1;19(11):1207-12; discussion 13. doi: 10.1097/00007632-199405310-00002.

Reference Type BACKGROUND
PMID: 8073311 (View on PubMed)

Brown MD, Lockwood JM. Degenerative spondylolisthesis. Instr Course Lect. 1983;32:162-9.

Reference Type BACKGROUND
PMID: 6546064 (View on PubMed)

Kostuik JP, Harrington I, Alexander D, Rand W, Evans D. Cauda equina syndrome and lumbar disc herniation. J Bone Joint Surg Am. 1986 Mar;68(3):386-91.

Reference Type BACKGROUND
PMID: 2936744 (View on PubMed)

Magora A. Conservative treatment in spondylolisthesis. Clin Orthop Relat Res. 1976 Jun;(117):74-9.

Reference Type BACKGROUND
PMID: 132329 (View on PubMed)

Matsunaga S, Ijiri K, Hayashi K. Nonsurgically managed patients with degenerative spondylolisthesis: a 10- to 18-year follow-up study. J Neurosurg. 2000 Oct;93(2 Suppl):194-8. doi: 10.3171/spi.2000.93.2.0194.

Reference Type BACKGROUND
PMID: 11012048 (View on PubMed)

Herkowitz HN. Spine update. Degenerative lumbar spondylolisthesis. Spine (Phila Pa 1976). 1995 May 1;20(9):1084-90. doi: 10.1097/00007632-199505000-00018.

Reference Type BACKGROUND
PMID: 7631240 (View on PubMed)

Weinstein JN, Tosteson TD, Lurie JD, Tosteson AN, Blood E, Hanscom B, Herkowitz H, Cammisa F, Albert T, Boden SD, Hilibrand A, Goldberg H, Berven S, An H; SPORT Investigators. Surgical versus nonsurgical therapy for lumbar spinal stenosis. N Engl J Med. 2008 Feb 21;358(8):794-810. doi: 10.1056/NEJMoa0707136.

Reference Type BACKGROUND
PMID: 18287602 (View on PubMed)

Atlas SJ, Keller RB, Robson D, Deyo RA, Singer DE. Surgical and nonsurgical management of lumbar spinal stenosis: four-year outcomes from the maine lumbar spine study. Spine (Phila Pa 1976). 2000 Mar 1;25(5):556-62. doi: 10.1097/00007632-200003010-00005.

Reference Type BACKGROUND
PMID: 10749631 (View on PubMed)

Herkowitz HN, Kurz LT. Degenerative lumbar spondylolisthesis with spinal stenosis. A prospective study comparing decompression with decompression and intertransverse process arthrodesis. J Bone Joint Surg Am. 1991 Jul;73(6):802-8.

Reference Type BACKGROUND
PMID: 2071615 (View on PubMed)

Gibson JN, Grant IC, Waddell G. The Cochrane review of surgery for lumbar disc prolapse and degenerative lumbar spondylosis. Spine (Phila Pa 1976). 1999 Sep 1;24(17):1820-32. doi: 10.1097/00007632-199909010-00012.

Reference Type BACKGROUND
PMID: 10488513 (View on PubMed)

Fischgrund JS, Mackay M, Herkowitz HN, Brower R, Montgomery DM, Kurz LT. 1997 Volvo Award winner in clinical studies. Degenerative lumbar spondylolisthesis with spinal stenosis: a prospective, randomized study comparing decompressive laminectomy and arthrodesis with and without spinal instrumentation. Spine (Phila Pa 1976). 1997 Dec 15;22(24):2807-12. doi: 10.1097/00007632-199712150-00003.

Reference Type BACKGROUND
PMID: 9431616 (View on PubMed)

Kornblum MB, Fischgrund JS, Herkowitz HN, Abraham DA, Berkower DL, Ditkoff JS. Degenerative lumbar spondylolisthesis with spinal stenosis: a prospective long-term study comparing fusion and pseudarthrosis. Spine (Phila Pa 1976). 2004 Apr 1;29(7):726-33; discussion 733-4. doi: 10.1097/01.brs.0000119398.22620.92.

Reference Type BACKGROUND
PMID: 15087793 (View on PubMed)

Bono CM, Lee CK. Critical analysis of trends in fusion for degenerative disc disease over the past 20 years: influence of technique on fusion rate and clinical outcome. Spine (Phila Pa 1976). 2004 Feb 15;29(4):455-63; discussion Z5. doi: 10.1097/01.brs.0000090825.94611.28.

Reference Type BACKGROUND
PMID: 15094543 (View on PubMed)

Ray CD. Threaded titanium cages for lumbar interbody fusions. Spine (Phila Pa 1976). 1997 Mar 15;22(6):667-79; discussion 679-80. doi: 10.1097/00007632-199703150-00019.

Reference Type BACKGROUND
PMID: 9089940 (View on PubMed)

Ekman P, Moller H, Tullberg T, Neumann P, Hedlund R. Posterior lumbar interbody fusion versus posterolateral fusion in adult isthmic spondylolisthesis. Spine (Phila Pa 1976). 2007 Sep 15;32(20):2178-83. doi: 10.1097/BRS.0b013e31814b1bd8.

Reference Type BACKGROUND
PMID: 17873808 (View on PubMed)

Kim KT, Lee SH, Lee YH, Bae SC, Suk KS. Clinical outcomes of 3 fusion methods through the posterior approach in the lumbar spine. Spine (Phila Pa 1976). 2006 May 20;31(12):1351-7; discussion 1358. doi: 10.1097/01.brs.0000218635.14571.55.

Reference Type BACKGROUND
PMID: 16721298 (View on PubMed)

Dantas FL, Prandini MN, Ferreira MA. Comparison between posterior lumbar fusion with pedicle screws and posterior lumbar interbody fusion with pedicle screws in adult spondylolisthesis. Arq Neuropsiquiatr. 2007 Sep;65(3B):764-70. doi: 10.1590/s0004-282x2007000500006.

Reference Type BACKGROUND
PMID: 17952277 (View on PubMed)

La Rosa G, Cacciola F, Conti A, Cardali S, La Torre D, Gambadauro NM, Tomasello F. Posterior fusion compared with posterior interbody fusion in segmental spinal fixation for adult spondylolisthesis. Neurosurg Focus. 2001 Apr 15;10(4):E9. doi: 10.3171/foc.2001.10.4.10.

Reference Type BACKGROUND
PMID: 16732636 (View on PubMed)

Humphreys SC, Hodges SD, Patwardhan AG, Eck JC, Murphy RB, Covington LA. Comparison of posterior and transforaminal approaches to lumbar interbody fusion. Spine (Phila Pa 1976). 2001 Mar 1;26(5):567-71. doi: 10.1097/00007632-200103010-00023.

Reference Type BACKGROUND
PMID: 11242386 (View on PubMed)

Hackenberg L, Halm H, Bullmann V, Vieth V, Schneider M, Liljenqvist U. Transforaminal lumbar interbody fusion: a safe technique with satisfactory three to five year results. Eur Spine J. 2005 Aug;14(6):551-8. doi: 10.1007/s00586-004-0830-1. Epub 2005 Jan 26.

Reference Type BACKGROUND
PMID: 15672243 (View on PubMed)

Hee HT, Castro FP Jr, Majd ME, Holt RT, Myers L. Anterior/posterior lumbar fusion versus transforaminal lumbar interbody fusion: analysis of complications and predictive factors. J Spinal Disord. 2001 Dec;14(6):533-40. doi: 10.1097/00002517-200112000-00013.

Reference Type BACKGROUND
PMID: 11723406 (View on PubMed)

Lauber S, Schulte TL, Liljenqvist U, Halm H, Hackenberg L. Clinical and radiologic 2-4-year results of transforaminal lumbar interbody fusion in degenerative and isthmic spondylolisthesis grades 1 and 2. Spine (Phila Pa 1976). 2006 Jul 1;31(15):1693-8. doi: 10.1097/01.brs.0000224530.08481.4e.

Reference Type BACKGROUND
PMID: 16816765 (View on PubMed)

Lowe TG, Tahernia AD. Unilateral transforaminal posterior lumbar interbody fusion. Clin Orthop Relat Res. 2002 Jan;(394):64-72. doi: 10.1097/00003086-200201000-00008.

Reference Type BACKGROUND
PMID: 11795753 (View on PubMed)

McAfee PC, DeVine JG, Chaput CD, Prybis BG, Fedder IL, Cunningham BW, Farrell DJ, Hess SJ, Vigna FE. The indications for interbody fusion cages in the treatment of spondylolisthesis: analysis of 120 cases. Spine (Phila Pa 1976). 2005 Mar 15;30(6 Suppl):S60-5. doi: 10.1097/01.brs.0000155578.62680.dd.

Reference Type BACKGROUND
PMID: 15767888 (View on PubMed)

Potter BK, Freedman BA, Verwiebe EG, Hall JM, Polly DW Jr, Kuklo TR. Transforaminal lumbar interbody fusion: clinical and radiographic results and complications in 100 consecutive patients. J Spinal Disord Tech. 2005 Aug;18(4):337-46. doi: 10.1097/01.bsd.0000166642.69189.45.

Reference Type BACKGROUND
PMID: 16021015 (View on PubMed)

Salehi SA, Tawk R, Ganju A, LaMarca F, Liu JC, Ondra SL. Transforaminal lumbar interbody fusion: surgical technique and results in 24 patients. Neurosurgery. 2004 Feb;54(2):368-74; discussion 374. doi: 10.1227/01.neu.0000103493.25162.18.

Reference Type BACKGROUND
PMID: 14744283 (View on PubMed)

Umehara S, Zindrick MR, Patwardhan AG, Havey RM, Vrbos LA, Knight GW, Miyano S, Kirincic M, Kaneda K, Lorenz MA. The biomechanical effect of postoperative hypolordosis in instrumented lumbar fusion on instrumented and adjacent spinal segments. Spine (Phila Pa 1976). 2000 Jul 1;25(13):1617-24. doi: 10.1097/00007632-200007010-00004.

Reference Type BACKGROUND
PMID: 10870136 (View on PubMed)

Kumar MN, Baklanov A, Chopin D. Correlation between sagittal plane changes and adjacent segment degeneration following lumbar spine fusion. Eur Spine J. 2001 Aug;10(4):314-9. doi: 10.1007/s005860000239.

Reference Type BACKGROUND
PMID: 11563617 (View on PubMed)

Champain S, Benchikh K, Nogier A, Mazel C, Guise JD, Skalli W. Validation of new clinical quantitative analysis software applicable in spine orthopaedic studies. Eur Spine J. 2006 Jun;15(6):982-91. doi: 10.1007/s00586-005-0927-1. Epub 2005 Jun 17.

Reference Type BACKGROUND
PMID: 15965708 (View on PubMed)

Bridwell KH, Lenke LG, McEnery KW, Baldus C, Blanke K. Anterior fresh frozen structural allografts in the thoracic and lumbar spine. Do they work if combined with posterior fusion and instrumentation in adult patients with kyphosis or anterior column defects? Spine (Phila Pa 1976). 1995 Jun 15;20(12):1410-8.

Reference Type BACKGROUND
PMID: 7676341 (View on PubMed)

Rillardon L, Levassor N, Guigui P, Wodecki P, Cardinne L, Templier A, Skalli W. [Validation of a tool to measure pelvic and spinal parameters of sagittal balance]. Rev Chir Orthop Reparatrice Appar Mot. 2003 May;89(3):218-27. French.

Reference Type BACKGROUND
PMID: 12844045 (View on PubMed)

Fairbank JC, Couper J, Davies JB, O'Brien JP. The Oswestry low back pain disability questionnaire. Physiotherapy. 1980 Aug;66(8):271-3. No abstract available.

Reference Type BACKGROUND
PMID: 6450426 (View on PubMed)

Prolo DJ, Oklund SA, Butcher M. Toward uniformity in evaluating results of lumbar spine operations. A paradigm applied to posterior lumbar interbody fusions. Spine (Phila Pa 1976). 1986 Jul-Aug;11(6):601-6. doi: 10.1097/00007632-198607000-00012.

Reference Type BACKGROUND
PMID: 3787326 (View on PubMed)

Ware JE Jr, Sherbourne CD. The MOS 36-item short-form health survey (SF-36). I. Conceptual framework and item selection. Med Care. 1992 Jun;30(6):473-83.

Reference Type BACKGROUND
PMID: 1593914 (View on PubMed)

Finlay AY. Quality of life assessments in dermatology. Semin Cutan Med Surg. 1998 Dec;17(4):291-6. doi: 10.1016/s1085-5629(98)80026-6.

Reference Type BACKGROUND
PMID: 9859917 (View on PubMed)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

CHUBX 2008/33

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.