Clinical Trial

Functioning in Individuals with Cervical Radiculopathy After Posterior Cervical Decompression

Recruiting
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Record status
This record was last updated November 25, 2024 (before its estimated December 31, 2025 completion). Its status may not reflect the trial's current state.
Summary
Compression on structures, as spinal nerves, in the cervical spine can cause cervical radiculopathy which leads to pain, disability, and reduced quality of life for the affected individual. Cervical foraminotomy with our without laminectomy are common posterior decompression surgical techniques for treating cervical radiculopathy. There is a lack of knowledge regarding function in patients with cervical radiculopathy after posterior cervical decompression. The aim with this study is to study pain, function, psychosocial factors, and health related quality of life after posterior cervical decompression in patients with cervical radiculopathy. This is a prospective multicenter longitudinal observational cohort study with follow-up at three, 12- and 24 months postoperative. A total of 154 individuals scheduled to undergo foraminotomy with our without laminectomy due to cervical radiculopathy will be included. Primary outcome is neck-specific function measured with the Neck Disability Index. Data will be collected preoperatively and at three, 12 and 24 months with electronic questionnaire.
Protocol Amendment History 2 amendments
This ClinicalTrials.gov record has been amended 2 times since 2022-03-25; most recent amendment 2024-11-21.
Status change: Not Yet Recruiting → Recruiting 2023-10-23
Trial Details
NCT Number NCT05310578
Lead Sponsor Linkoeping University
Conditions Cervical Radiculopathy
Enrollment 154 participants
Start Date 2022-08-22
Primary Completion 2025-12-31 (estimated)
Study Completion 2025-12-31 (estimated)
Updated on ClinicalTrials.gov 2024-11-25