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A study to assess the effect after video assisted shoulder ligament surgery

Assessment of Safety, Efficacy, and Functional Outcomes after Rotator Cuff Repair using Ceptre® Titanium Screw Anchor: A Single Centre, Retrospective, Observational Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2022/10/046852
Enrollment
40
Registered
2022-10-27
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. Patients aged =18 years who has undergone rotator cuff repair surgery with Ceptre® Titanium Screw Anchor between January 2019 to July 2022. 2. Patients willing to give written consent for the study during an in-clinic visit or providing verbal consent for participation during a telephonic visit

Exclusion criteria

Exclusion criteria: 1. Patients who suffered from traumatic injury to the operated shoulder after surgery. 2. Patients who cannot be contacted after three attempts

Design outcomes

Primary

MeasureTime frame
To evaluate the functional outcomes after Rotator Cuff Repair with Ceptre® Titanium Screw AnchorTimepoint: At baseline—

Secondary

MeasureTime frame
1. To review the safety of Ceptre® Titanium Screw Anchor by evaluating adverse events after surgery. 2. To review the efficacy of Ceptre® Titanium Screw Anchor after Rotator Cuff Repair.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