A study to assess success after repair of knee ligament injury

A Single Centre, Retrospective, Observational Study to Assess the Safety and Functional Outcomes after Arthroscopic Meniscal repair using Surestitch All inside meniscal repair implant

Status

Active, not recruiting

Phases

Phase 4

Study type

Observational

Source

CTRI

Registry ID

CTRI/2022/10/046810

Enrollment

Registered

2022-10-26

Start date

Unknown

Completion date

Unknown

Last updated

2023-11-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients aged =18 years who has undergone meniscal repair surgery with Surestitch All-inside meniscal repair implant, between January 2019 to July 2022. 2. Patients willing to give written informed consent for the study during an in-clinic follow-up visit or provide verbal consent for the study during a telephonic follow-up visit.

Exclusion criteria

Exclusion criteria: 1. Patients who have suffered from Traumatic injury to the same knee after meniscus repair surgery 2. Patients who cannot be contacted after 3 attempts

Design outcomes

Primary

Measure	Time frame
To evaluate the postoperative subjective knee function after meniscal repair using Surestitch implants.Timepoint: At baseline	—

Secondary

Measure	Time frame
1. To review the safety of Surestitch implants in meniscal repair by evaluating adverse events after surgery. 2. To compare the activity level in patients before and after meniscal repair. 3. To evaluate the knee pain after meniscal repair. 4. To evaluate the knee specific symptoms after meniscal repair.Timepoint: At baseline	—

Countries

India

Contacts

Public ContactDr Ashok Kumar Moharana

Healthium Medtech Limited

ashok.m@healthiummedtech.com9717887751

Outcome results