The Effect of Using Autologous Platelet Rich Plasma on Posterior Lumbar Interbody Fusion

NCT ID: NCT03261843

Last Updated: 2017-08-25

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

UNKNOWN

Clinical Phase

PHASE4

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-11-01

Study Completion Date

2019-05-01

Brief Summary

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

the study aims to determine the effect of using Autologous platelet rich plasma on both the quality \& rate of posterior lumbar interbody fusion \& its outcome on the Patient regarding postoperative lumbar pain \& functional outcome

Detailed Description

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

The study will be submitted for approval by the Ethics Committee of Faculty of Medicine, Assiut University, and written informed consent will be obtained from all patients prior to enrollment. The study population will be selected from patients attending the Department of Orthopedics and Trauma surgery, Assiut University hospitals.

Sixty patients will be selected for the study and will be randomized into two group one receiving posterior lumbar interbody fusion with Autologous platelet rich plasma and the other group will receive posterior lumbar interbody fusion without Autologous platelet rich plasma.

Methodology pre-operative preparation: Prior to the operation the selected patients will perform lumbar spine Computarised tomography and X ray films. Both the visual analogue scale of pain and the Oswestry disability index will be collected from the patients

Autologous platelet rich plasma preparation:

Autologous Platelet rich plasma is obtained using a two-stage centrifugation process.

Whole blood sample will be drawn from the participant and be collected in a sterile tube containing anticoagulant (sodium citrate 3.8% or Ethylenediaminetetraacetic acid ). The tube will be centrifuged at 160xg relative centrifugal force (about 1000 round per minute) for 10 min in a centrifugal apparatus. The first spin will separate platelet poor plasma at the top from red blood cells at the bottom and platelet rich plasma above (mixed with the white blood cells in the buffy coat). The Platelet poor plasma, Platelet rich plasma and a few red blood cells will be aspirated into a new tube, mixed and in the second spin, the tube will be centrifuged at 400xg relative centrifugal form (about 1500 round per minute) for another 10 minutes. The upper section will consist of Platelet poor plasma and the Platelet rich plasma will be collected at the bottom of the tube in the form of pellet. Then, Platelet poor plasma and Platelet rich plasma will be aspirated and mixed (discarding the upper portion). Prior to treatment calcium chloride 3% will be added to activate platelets immediately before its application to avoid coagulation of the specimen (for every 1.5 milliliter plasma, 1 milliliter calcium chloride 3% is added).

Surgery:

A posterior lumbar interbody fusion with posterior pedicle screw fixation will be performed through a midline posterior approach. Trans-pedicular screws will be placed under fluoroscopic guidance, followed by discectomy. The vertebral body endplates will be prepared by curetting until point bleeding was seen.

Autologous cancellous bone chips will be harvested unilaterally from the iliac wing, approached through the midline posterior incision. The bone chips will be steeped in the plasma solution until clotting occurred visually (approximately 10 minutes). In the control group, the bone chips will be filled with autologous bone in the same way and were implanted after approximately 10 minutes without incubation in a plasma solution.

Conditions

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

Autologous Platelet Rich Plasma Effect on Bone Healing

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

single center, prospective randomized comparative trial
Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors
the person performing the statistical analysis shall be masked

Study Groups

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

posterior lumbar interbody fusion + platelet rich plasma

the addition of autologous platelet rich plasma to the bone graft

Group Type ACTIVE_COMPARATOR

autologous platelet rich plasma

Intervention Type BIOLOGICAL

adding autologous platelet rich plasma to the bone graft harvested from the patient

posterior lumbar interbody fusion

bone graft alone

Group Type ACTIVE_COMPARATOR

posterior lumbar interbody fusion without autologous platelet rich plasma

Intervention Type PROCEDURE

performing posterior lumbar interbody fusion without using platelet rich plasma

Interventions

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

autologous platelet rich plasma

adding autologous platelet rich plasma to the bone graft harvested from the patient

Intervention Type BIOLOGICAL

posterior lumbar interbody fusion without autologous platelet rich plasma

performing posterior lumbar interbody fusion without using platelet rich plasma

Intervention Type PROCEDURE

Eligibility Criteria

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

Inclusion Criteria

* Spondylolisthesis.
* Degenerative disc disease requiring posterior lumbar interbody fusion not responding to medical treatment for 1 year.
* Age between 20 \& 70 years.
* Single or multiple level fusions.

Exclusion Criteria

* Previous lumbar spine surgery.
* Other lumbar spine pathology
* severe osteoporosis
* Chronic use of steroid or non-steroidal anti-inflammatory drugs (more than one year)
* Patients younger than 20 years old.
* Patients older than 70 years old.
* Immunocompromised patients (eg. Chronic renal failure)
Minimum Eligible Age

20 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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

Assiut University

OTHER

Sponsor Role lead

Responsible Party

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

Ahmed Abdelazim Abdelrahim Hassan

resident of orthopedics and trauma surgery

Responsibility Role PRINCIPAL_INVESTIGATOR

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Ahmed A A Hassan, M.B.B.ch

Role: CONTACT

+201288103657

References

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

Smith PA. Intra-articular Autologous Conditioned Plasma Injections Provide Safe and Efficacious Treatment for Knee Osteoarthritis: An FDA-Sanctioned, Randomized, Double-blind, Placebo-controlled Clinical Trial. Am J Sports Med. 2016 Apr;44(4):884-91. doi: 10.1177/0363546515624678. Epub 2016 Feb 1.

Reference Type RESULT
PMID: 26831629 (View on PubMed)

Sys J, Weyler J, Van Der Zijden T, Parizel P, Michielsen J. Platelet-rich plasma in mono-segmental posterior lumbar interbody fusion. Eur Spine J. 2011 Oct;20(10):1650-7. doi: 10.1007/s00586-011-1897-0. Epub 2011 Jul 10.

Reference Type RESULT
PMID: 21744284 (View on PubMed)

Weiner BK, Walker M. Efficacy of autologous growth factors in lumbar intertransverse fusions. Spine (Phila Pa 1976). 2003 Sep 1;28(17):1968-70; discussion 1971. doi: 10.1097/01.BRS.0000083141.02027.48.

Reference Type RESULT
PMID: 12973143 (View on PubMed)

Hee HT, Majd ME, Holt RT, Myers L. Do autologous growth factors enhance transforaminal lumbar interbody fusion? Eur Spine J. 2003 Aug;12(4):400-7. doi: 10.1007/s00586-003-0548-5. Epub 2003 May 22.

Reference Type RESULT
PMID: 12761669 (View on PubMed)

Kaux JF, Le Goff C, Seidel L, Peters P, Gothot A, Albert A, Crielaard JM. [Comparative study of five techniques of preparation of platelet-rich plasma]. Pathol Biol (Paris). 2011 Jun;59(3):157-60. doi: 10.1016/j.patbio.2009.04.007. Epub 2009 May 28. French.

Reference Type RESULT
PMID: 19481375 (View on PubMed)

Marx RE. Platelet-rich plasma: evidence to support its use. J Oral Maxillofac Surg. 2004 Apr;62(4):489-96. doi: 10.1016/j.joms.2003.12.003. No abstract available.

Reference Type RESULT
PMID: 15085519 (View on PubMed)

Ferrari M, Zia S, Valbonesi M, Henriquet F, Venere G, Spagnolo S, Grasso MA, Panzani I. A new technique for hemodilution, preparation of autologous platelet-rich plasma and intraoperative blood salvage in cardiac surgery. Int J Artif Organs. 1987 Jan;10(1):47-50.

Reference Type RESULT
PMID: 3570542 (View on PubMed)

Other Identifiers

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

platelet rich plasma

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

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

LUMBAR & SACROILIAC FUSION STUDY
NCT07204288 RECRUITING NA
Intradiscal Platelet Rich Plasma
NCT04544709 TERMINATED PHASE4