Anterior cervical spine fusion study
Not Applicable
- Conditions
- Health Condition 1: M509- Cervical disc disorder, unspecified
- Registration Number
- CTRI/2021/01/030690
- Lead Sponsor
- Sakra World Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients with Degenerative disease of the cervical spine and
•Radiculopathy
•Myelopathy
•Kyphosis and disability
Exclusion Criteria
•Infections / Trauma requiring ACDF
•ACDF Procedures combined with posterior surgeries
•Patients with more than 2 level pathology
•Severe medical co-morbidities precluding surgery
•Patients who have undergone surgery in Cervical region previously
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method FusionTimepoint: Baseline,1,3,6,12 months
- Secondary Outcome Measures
Name Time Method Visual Analogue Scale (VAS) score pain assessment, mJOA (modified Japanese Orthopaedic Association) score, NDI (Neck disability index) and Odomâ??s criteriaTimepoint: Baseline,1,3,6,12 months