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A study to assess result after shoulder surgery

A Prospective, Multicentric, Single-arm Study to evaluate the effectiveness and safety in Patients undergoing Arthroscopic Bankarts Repair using Knotted UHMWPE Suture Anchor.

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/07/055473
Enrollment
44
Registered
2023-07-21
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Health Condition 1: M999- Biomechanical lesion, unspecified

Interventions

Intervention1: Stativ Knotted UHMWPE Suture Anchor: Stativ Knotted UHMWPE Suture Anchor is used for soft tissue fixation by the use of sutures to bone. (Duration: Its a permanent implant and will not

Sponsors

Healthium Medtech Limited
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Male and female subjects between 18 to 40 years of age. 2.Subjects with Bankarts lesion requiring primary Arthroscopic Bankarts repair surgery. 3.Subjects willing to give written informed consent to participate in the study.

Exclusion criteria

Exclusion criteria: 1.Subjects with BMI =35 kg/m2. 2.Subjects with history of any surgery to the same shoulder. 3.Subjects with active infection or blood supply limitations. 4.Subjects with pathological conditions of bone or soft tissue that would impair secure fixation. 5.Subjects with known hypersensitivity to UHMWPE 6.Subjects with conditions, which would limit the subjects ability or willingness to restrict activities or follow directions during the healing period. 7.Subjects having any condition that could affect healing (eg. Infections, Regular use of Corticosteroids, Diabetes – HbA1C = 10). 8.Subjects with history of heavy smoking (= 20 cigarettes/day) within the last 6 months. 9.Subjects with a medical or physical condition that, in the opinion of the Investigator, would preclude safe subject participation in the study 10.Subjects who are pregnant or lactating at the time of screening.

Design outcomes

Primary

MeasureTime frame
To assess the shoulder function and stability post Bankarts repair using Knotted UHMWPE Suture AnchorTimepoint: Baseline, 3 months post-surgery, 6 months post-surgery, 12 months post-surgery, 18 months post-surgery, and 24 months post-surgery

Secondary

MeasureTime frame
1.To assess the functional outcomes post Bankarts repair using Knotted UHMWPE Suture Anchor 2.To assess the instability after Bankart’s repair using Knotted UHMWPE Suture Anchor 3.To assess the failure rate of Bankart’s repair using Knotted UHMWPE Suture Anchor 4.To assess change in quality of life post Bankarts repair using Knotted UHMWPE Suture Anchor 5.To assess the time to recovery post Bankarts repair using Knotted UHMWPE Suture Anchor 6.To assess the overall intraoperative handling of Knotted UHMWPE Suture Anchor 7.To evaluate the ligament and implant condition after Arthroscopic Bankarts repair surgery 8.To assess the incidence of residual risks and safety of Knotted UHMWPE Suture AnchorTimepoint: Day of surgery, Day of Discharge, 15th day post-surgery, 3 months post-surgery, 6 months post-surgery, 12 months post-surgery, 18 months post-surgery, and 24 months post-surgery

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