A study to assess success after shoulder ligament repair surgery
Not Applicable
Completed
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2022/12/048062
- Lead Sponsor
- Healthium Medtech Limited
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Male/ Female Patients of 18 to 80 years of age.
2. Patients who underwent arthroscopic rotator cuff tears repair using Sironix suture anchor between the period of January 2019 to June 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 traumatic injury to the same shoulder post rotator cuff tears repair procedure.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate the function of the shoulder after Arthroscopic Rotator Cuff Tears RepairTimepoint: One followup after EC approval 3 months to 3.5 years after surgery
- Secondary Outcome Measures
Name Time Method 1. To assess the level of activity pre and post-surgery <br/ ><br>2. To assess quality of life after Rotator Cuff Tears Repair <br/ ><br>3. To assess the adverse events associated with Arthroscopic Rotator Cuff Tears Repair <br/ ><br>Timepoint: One followup after EC approval 3 months to 3.5 years after surgery