CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 138 enrolled
Drug / intervention
HEALICOIL Knotless PEEK +1 moredevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04552119
NCT04552119N/ACompleted
CompareCT.gov

Prospective, Multi-Center, Post-Market Clinical Follow-up Study to Evaluate Safety and Performance of the HEALICOIL™ Knotless Suture Anchor in Shoulder Rotator Cuff Tendon Repair

Smith & Nephew, Inc.·observational·Posted Sep 17, 2020·Updated Apr 16, 2026

In Brief

An observational study evaluating HEALICOIL Knotless PEEK and HEALICOIL Knotless REGENESORB for Rotator Cuff. Completed, enrolled 138 participants across 5 sites.

Detailed Summary

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

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsRotator Cuff
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
202120222023202420252026
First PostedSep 17, 2020
Enrollment StartJan 26, 2021
Primary CompletionMay 24, 2024
TodayJul 2, 2026
Enrollment to primary: 3.3 yearsPosted 5.8 years ago

Interventions

HEALICOIL Knotless PEEKdevice

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

HEALICOIL Knotless REGENESORBdevice

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