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Collagen Scaffold

Partial Rotator Cuff Repair with Regeneten Scaffold for Rotator Cuff Tears

N/A
Waitlist Available
Research Sponsored by Rothman Institute Orthopaedics
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 24 months
Awards & highlights

Study Summary

This study is evaluating whether a scaffold can improve the outcome of rotator cuff repair.

Eligible Conditions
  • Rotator Cuff Tears
  • Shoulder Surgery

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~24 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and 24 months for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Participant Satisfaction: ASES assessment
Participant Satisfaction: GRC assessment
Participant Satisfaction: SANE assessment
+3 more

Trial Design

2Treatment groups
Active Control
Group I: Partial Rotator Cuff RepairActive Control1 Intervention
Routine partial rotator cuff repair
Group II: Partial Rotator Cuff Repair with Regeneten ScaffoldActive Control1 Intervention
Routine partial rotator cuff repair with the addition of the Regeneten scaffolding patch

Find a Location

Who is running the clinical trial?

Rothman Institute OrthopaedicsLead Sponsor
121 Previous Clinical Trials
21,498 Total Patients Enrolled
3 Trials studying Rotator Cuff Tears
268 Patients Enrolled for Rotator Cuff Tears

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Recent research and studies
clinicaltrials.govStudy
Regeneten Patch vs Standard Care in Partial Thickness Rotator Cuff Repair
2020. "Regeneten Patch vs Standard Care in Partial Thickness Rotator Cuff Repair". ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT04673344.
~18 spots leftby May 2025
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