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ropivacaine 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 surgery through 48 hours post-op
Awards & highlights

Study Summary

This trial is testing whether a different kind of painkiller can reduce the amount of post-operative narcotics a patient needs.

Eligible Conditions
  • Rotator Cuff Tears

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~surgery through 48 hours post-op
This trial's timeline: 3 weeks for screening, Varies for treatment, and surgery through 48 hours post-op for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
opioid consumption

Trial Design

2Treatment groups
Active Control
Group I: ropivacaineActive Control1 Intervention
Group II: liposomal bupivacaineActive Control1 Intervention

Find a Location

Who is running the clinical trial?

Rothman Institute OrthopaedicsLead Sponsor
121 Previous Clinical Trials
21,446 Total Patients Enrolled
3 Trials studying Rotator Cuff Tears
216 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
Post-operative Exparel Study Following Rotator Cuff Repair
2019. "Post-operative Exparel Study Following Rotator Cuff Repair". ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT04047745.
All > Exparel
~24 spots leftby Apr 2025
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