A study to assess ooutcomes after knee ligament surgery
Not Applicable
Completed
- Conditions
- Health Condition 1: M259- Joint disorder, unspecified
- Registration Number
- CTRI/2022/12/048128
- Lead Sponsor
- Healthium Medtech Limited
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 32
Inclusion Criteria
1. Male/ Female Patients of 18 to 60 years of age
2. Patients who underwent arthroscopic anterior cruciate ligament (ACL) reconstruction using Sironix suture button and/or interference screw between the period of January 2018 to March 2022
3. Patient willing to give written informed consent to participate in the study when attending an in-clinic follow-up visit, or providing verbal consent during the telephonic follow-up visit
Exclusion Criteria
1. Patients not responding to calls after three attempts or not interested to participate in the study
2. Patients with injury or re-surgery to the same knee post ACL reconstruction procedure
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method