A study to assess outcomes after knee surgery
Not Applicable
Completed
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/10/059136
- Lead Sponsor
- Healthium Medtech Limited
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 47
Inclusion Criteria
1.Male/female participants aged =18 to =60 years at the time of surgery
2. Participants who had undergone arthroscopic ACL reconstruction procedure using adjustable PEEK Button at least one month prior to their follow-up
3. Participants who are willing to provide written informed consent (in case of physical visit to the site) or verbal informed consent (in case of telephonic visit)
Exclusion Criteria
1.Participants who have suffered traumatic injury to the operated knee post ACL reconstruction procedure
2. Participants who are not willing to attend the follow-up
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method