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A study to assess success and failure after knee ligament surgery

A retrospective, single centre, observational study to evaluate the safety, clinical outcomes and patient reported outcomes after meniscus repair using Surestitch all inside meniscal repair implant.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2022/11/047637
Enrollment
50
Registered
2022-11-24
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

Sponsors

Healthium Medtech Limited
Lead Sponsor

Eligibility

Inclusion criteria

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

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.

Design outcomes

Primary

MeasureTime frame
To evaluate the clinical outcomes after meniscus repair using Surestitch all inside meniscal repair implant.Timepoint: At baseline—

Secondary

MeasureTime frame
1. To evaluate the patient reported outcomes after meniscus repair using Surestitch all inside meniscal repair implant 2. To evaluate the safety of the SURESTITCH™ meniscal repair implant after meniscus repair surgery. Timepoint: At baseline—

Countries

India

Contacts

Public ContactDr Ashok Kumar Moharana

Healthium Medtech Limited

ashok.m@healthiummedtech.com9717887751

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026