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Enrolling By InvitationNCT06868108

Clinical Trial on the Effect of the Flexible Suturing System With Anchors (FSSA) in Full-thickness Rotator Cuff Tendon Tears

Status
Enrolling By Invitation
Phase
Study type
Observational
Enrollment
100 (estimated)
Sponsor
Integrity Orthopaedics, Inc. · Industry
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

The purpose of this research study is to evaluate tendon healing when using the Flexible Suturing System with Anchors (FSSA) to surgically repair full-thickness rotator cuff tendon tears.

Conditions

Interventions

TypeNameDescription
DEVICEFlexible Suturing System with Anchors (FSSA)Surgically repaired full-thickness rotator cuff tendon tears with the Flexible Suturing System with Anchors (FSSA).

Timeline

Start date
2025-02-20
Primary completion
2025-12-01
Completion
2025-12-01
First posted
2025-03-10
Last updated
2025-09-10

Locations

3 sites across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT06868108. Inclusion in this directory is not an endorsement.

Clinical Trial on the Effect of the Flexible Suturing System With Anchors (FSSA) in Full-thickness Rotator Cuff Tendon T (NCT06868108) · Clinical Trials Directory