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Safety of Treatment of Shoulder Repair

NCT04552119 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 138

Last updated 2026-04-16

Study results available
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Summary

This study evaluates the safety of the HEALICOIL Knotless Suture Anchors in patients requiring a repair of the rotator cuff tendon repair

Conditions

  • Rotator Cuff

Interventions

DEVICE

HEALICOIL Knotless PEEK

HEALICOIL Knotless PEEK Self-Tapping HEALICOIL Knotless Non-Self Tapping

DEVICE

HEALICOIL Knotless REGENESORB

HEALICOIL Knotless REGENESORB Self -Tapping HEALICOIL Knotless REGENSORB Non-Self Tapping

Sponsors & Collaborators

  • Smith & Nephew, Inc.

    lead INDUSTRY

Principal Investigators

  • Karlie Morgan · Smith & Nephew, Inc.

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-01-26
Primary Completion
2024-05-24
Completion
2024-05-24
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04552119 on ClinicalTrials.gov