Occipito-Cervical Stabilization Using Occipital Condyle Screw

NCT ID: NCT03250611

Last Updated: 2017-08-15

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

NA

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-09-30

Study Completion Date

2020-01-31

Brief Summary

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

The Occipito-Cervical (OC) junction is the most cephalad portion of the spinal axis, with anatomical osseous complex that allows significant mobility while maintaining biomechanical stability. OC instability is a rare disorder with potentially life-threatening consequences. Instability may manifest as disabling pain, cranial nerve dysfunction, paralysis, or even sudden death. The most common acute presentation is secondary to major trauma. Other pathologic processes that may lead to chronic instability include rheumatoid arthritis, infections, tumors, and even congenital malformations; OC fusion in aforementioned cases each according is then indicated.

Stabilization of the OC junction remains a challenge, owing to the regional anatomy and poor occipital bone purchase. OC stabilization techniques have undergone continuous refinement. Early techniques involving simple posterior only bone grafts demonstrated a high rate of failure and have largely been replaced by rigid posterior fixation systems using rods/screws or plates, providing superior biomechanical stability and higher rates of fusion. One of the very modern modalities of fixation methods is the Occipital Condyle Screw (OCS) as a sole cranial anchor; believing that decreasing the length of lever arm of the construct, increasing the length of the screw purchase, and decreasing stresses addressed on the rod with no need to excessively bend it for the occipital slope may enhance the construct rigidity, and leaving a greater clear metal-free area of the occiput for graft contact may have a real potential benefits in fusion rates.

Detailed Description

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

Clinical Evaluation: of patients with 1- Visual Analogue Scale (VAS), 2- Neck Disability Index (NDI), 3- Modified Japanese Orthopaedic Association Cervical Myelopathy Score (mJOA.CMS), 4- American Spinal Injury Association Score (ASIAs). Immediate preoperative functional scoring, and 6 weeks, 3 months, 6 months, and 1 year postoperative.

Surgical Technique: The patient is handled in prone position after successful general anaesthesia with supported head to ensure that the Occipito-Cervical junction maintains in neutral position. The Occipito-Cervical junction is then exposed through a traditional midline longitudinal posterior skin incision extends from the external occipital protuberance to the C3-C4 level. The nuchal ligament is divided in the midline, and the occipital and cervical musculature is dissected subperiosteally. The suboccipital and cervical paraspinous muscles are retracted laterally to expose the underlying bony architecture. The posterior arch of C1 is exposed and the dissection is continued laterally in a subperiosteal manner to identify the horizontal segment of the vertebral arteries (VAs) which is enveloped in a dense venous plexus. The atlanto-occipital joint capsule is to be approx. 3 mm. Cranial to the superior margin of tht VA. Attention is then focused on the foramen magnum. Using curettes, the atlanto-occipital membrane is gently dissected from the foramen magnum laterally until the medial aspect of the occipital condyle is reached. At this point, the dissection continues laterally, maintaining bone contact to prevent injury to the horizontal segment of the VA along the condylar fossa, until the posterior condylar foramen and emissary vein are identified. The condylar foramen and vein represent the lateral extent of the dissection. At this stage, the operative field is prepared for instrumentation. Inserting the cervical screws first provides useful information about the axial location of the occipital condyles. The condylar entry point (CEP) is defined using a combination of radiographic and anatomic landmarks. The CEP is located (4 to 5 mm) lateral to the posteromedial edge of the condyle, and (2 mm) above the atlanto-occipital joint line. Pilot hole is then made at the entry point using an awl with slight cranial angulation to avoid injury to the horizontal segment of the VA. The pilot hole is then drilled under image-guidance in a convergent trajectory with (12 to 22 degrees) of medial angulation and (5 degrees) cranial angulation in the sagittal plane with the tip of the drill directed toward the basion, advancing slowly until the anterior cortical edge of the condyle is breached. The hole is tapped, and a (3.5 mm) polyaxial screw of an appropriate length (30 to 34 mm) is inserted bicortically into the occipital condyle. Approximately (12 mm) portion of the screw remains superficial to the posterior cortex of the condyle, allowing the polyaxial portion of the screw to lie above the posterior arch of C1, minimizing any chance of irritation of the VA by the rods.

Radiological Evaluation: 1- Preoperative: Plain X-ray (PXR) Antero-posterior (AP) and Lateral (Lat.) views to study the upper cervical instability indices and measurements, Multi-Slice Computed Tomography (MSCT) to study the boney Occipito-Cervical architecture for any fractures or anomalies, CT Angiography (CTA) to study the vertebral artery for anomaly especially in the horizontal segment of the VA, and Magnetic Resonance Imaging (MRI) to study the spinal cord for any compression signs. 2- Postoperative: Immediate (PXR) AP. and Lat. views for overall global assessment of the reduction and the construct installation. Then at 3 months, 6 months, and 1 year after surgery with flexion extension lateral view bending stress films for assessment of stability. Immediate (MSCT) to study the crucial screws placement estate for any breaches or successfulness, and after 1year for assessment of the fusion rate achieved.

Serial Follow-Up: after 6 weeks for clinical evaluation and functional scoring. At 3 and 6 months for radiological evaluation of stability, clinical evaluation and functional re-scoring. At 1 year for evaluation of fusion rate, clinical evaluation and over all resultant functional scores.

Conditions

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

Cervical Instabilities Spine

Study Design

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

Allocation Method

NA

Intervention Model

SINGLE_GROUP

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.

Occipito-Cervical Instability

Stabilization of the occipito-cervical junction by Occipital Condyle Screw (OCS) as a sole cranial anchor, with posterior bone graft.

Group Type EXPERIMENTAL

Occipital Condyle Screw

Intervention Type PROCEDURE

Occipito-Cervical Screw-Rod Fixation Technique

Interventions

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

Occipital Condyle Screw

Occipito-Cervical Screw-Rod Fixation Technique

Intervention Type PROCEDURE

Eligibility Criteria

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

Inclusion Criteria

* Patients with occipito-cervical instability of any cause, indicated for occipito-cervical fusion

Exclusion Criteria

* Fractured occipital condyle
* Congenital malformation of occipital condyle
* Congenital anomaly of the horizontal segment of the vertebral artery
Minimum Eligible Age

16 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.

Muhammad Almessry

Principal investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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

Mohamed El-Meshtawy, MD

Role: STUDY_DIRECTOR

Assiut University

Central Contacts

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

Ahmed Shawky, MD

Role: CONTACT

+201010212222

Muhammad Almessry, M.Sc.

Role: CONTACT

+201007262147

References

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

Uribe JS, Ramos E, Vale F. Feasibility of occipital condyle screw placement for occipitocervical fixation: a cadaveric study and description of a novel technique. J Spinal Disord Tech. 2008 Dec;21(8):540-6. doi: 10.1097/BSD.0b013e31816d655e.

Reference Type BACKGROUND
PMID: 19057245 (View on PubMed)

Uribe JS, Ramos E, Youssef AS, Levine N, Turner AW, Johnson WM, Vale FL. Craniocervical fixation with occipital condyle screws: biomechanical analysis of a novel technique. Spine (Phila Pa 1976). 2010 Apr 20;35(9):931-8. doi: 10.1097/BRS.0b013e3181c16f9a.

Reference Type BACKGROUND
PMID: 20375778 (View on PubMed)

Uribe JS, Ramos E, Baaj A, Youssef AS, Vale FL. Occipital cervical stabilization using occipital condyles for cranial fixation: technical case report. Neurosurgery. 2009 Dec;65(6):E1216-7; discussion E1217. doi: 10.1227/01.NEU.0000349207.98394.FA.

Reference Type BACKGROUND
PMID: 19934947 (View on PubMed)

La Marca F, Zubay G, Morrison T, Karahalios D. Cadaveric study for placement of occipital condyle screws: technique and effects on surrounding anatomic structures. J Neurosurg Spine. 2008 Oct;9(4):347-53. doi: 10.3171/SPI.2008.9.10.347.

Reference Type BACKGROUND
PMID: 18939920 (View on PubMed)

Ahmadian A, Dakwar E, Vale FL, Uribe JS. Occipitocervical fusion via occipital condylar fixation: a clinical case series. J Spinal Disord Tech. 2014 Jun;27(4):232-6. doi: 10.1097/BSD.0b013e31825bfeea.

Reference Type BACKGROUND
PMID: 24866907 (View on PubMed)

Tan GH, Goss BG, Thorpe PJ, Williams RP. CT-based classification of long spinal allograft fusion. Eur Spine J. 2007 Nov;16(11):1875-81. doi: 10.1007/s00586-007-0376-0. Epub 2007 May 12.

Reference Type BACKGROUND
PMID: 17497188 (View on PubMed)

Other Identifiers

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

OC.Screw

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

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

Spinal Cord Associative Plasticity Study
NCT05163639 RECRUITING EARLY_PHASE1
Cranio-spinal Neurosurgical Approaches
NCT07287462 NOT_YET_RECRUITING
Reanimation in Tetraplegia
NCT01997125 COMPLETED NA
Stem Cells in Spinal Cord Injury
NCT03935724 UNKNOWN PHASE2/PHASE3