An in-depth investigation and analysis were conducted on the real-world effectiveness of the Adaptix™ Interbody Cage System at a specialized spine center providing tertiary care.
Not Applicable
- Conditions
- Health Condition 1: M431- Spondylolisthesis
- Registration Number
- CTRI/2024/01/061495
- Lead Sponsor
- Stavya Spine Hospital and Research Institute
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All the cases who undergoing inter-body fusion with Adaptix™ inter-body system.
cases giving consent for surgery.
age group 18 and above
Exclusion Criteria
patients who are not willing to be a part of study.
Age below 18.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess the safety and performance of Adaptix™ through retrospective review of cases Done at our institute. <br/ ><br>To identify residual risk for Adaptix™. <br/ ><br>Identify off possible label use. <br/ ><br>Identify previously unknown side effects and complications. <br/ ><br>Timepoint: Visits at 3 months,6 months and 12 months
- Secondary Outcome Measures
Name Time Method ATimepoint: NA