MedPath

A study to assess success and failure after knee ligament surgery

Not Applicable
Completed
Conditions
Health Condition 1: O- Medical and Surgical
Registration Number
CTRI/2022/11/047637
Lead Sponsor
Healthium Medtech Limited
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
36
Inclusion Criteria

1. Male or Female patients with age of 18-80.

2. Patients who underwent meniscus repair with Surestitch meniscus repair implant between October 2020 to July 2022.

3. Able to give written informed consent during hospital visit or provide a verbal consent during a telephonic visit.

Exclusion Criteria

1. Patient who has suffered from traumatic injury to the operated knee after the meniscus repair surgery

2. Patient who cannot be contacted for attending an inclinic/telephonic follow-up visit.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To evaluate the clinical outcomes after meniscus repair using Surestitch all inside meniscal repair implant.Timepoint: At baseline
Secondary Outcome Measures
NameTimeMethod
1. To evaluate the patient reported outcomes after meniscus repair using Surestitch all inside meniscal repair implant <br/ ><br>2. To evaluate the safety of the SURESTITCH™ meniscal repair implant after meniscus repair surgery. <br/ ><br>Timepoint: At baseline
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