Hard Cervical Collar Use Following Posterior Cervical Fusion
NCT: NCT07789288 · RECRUITING
Brief Summary
Postoperative immobilization with a hard cervical collar following posterior cervical fusion remains common practice despite limited evidence demonstrating improved clinical outcomes. This is a prospective, multi-site, randomized clinical trial evaluating postoperative hard cervical collar use following posterior cervical fusion for degenerative cervical spine disease. Eligible patients will be randomized to either wear an FDA-approved hard cervical collar (Aspen Cervical Collar, Aspen Vista Cervical Collar, or Miami J Cervical Collar) for 6 weeks after surgery or receive no cervical collar. Patient-reported outcomes will be collected before surgery and at 2 weeks, 6 weeks, 12 weeks, 6 months, and 12 months after surgery. The primary outcome is radiographic fusion success at 12 months. Secondary outcomes include neck disability, neck and arm pain, quality of life, patient satisfaction, wound infection, adverse events, and other postoperative complications. Radiographic fusion will be evaluated by blinded radiologists. The results of this study will help determine whether routine postoperative cervical collar use improves outcomes following posterior cervical fusion.
Frequently Asked Questions
What is Hard Cervical Collar Use Following Posterior Cervical Fusion?
Hard Cervical Collar Use Following Posterior Cervical Fusion is a clinical trial registered under NCT07789288. Current status: RECRUITING.
What is the status of NCT07789288?
The current status of NCT07789288 (Hard Cervical Collar Use Following Posterior Cervical Fusion) is: RECRUITING.
When did Hard Cervical Collar Use Following Posterior Cervical Fusion start?
Hard Cervical Collar Use Following Posterior Cervical Fusion started on 2026-06-03.
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Official Source
View on ClinicalTrials.gov →Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.