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Pathway for Shoulder Pain

N/A
Waitlist Available
Led By Jacques YaDeau
Research Sponsored by Hospital for Special Surgery, New York
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 post op days 1,2,7,14
Awards & highlights

Study Summary

This study is evaluating whether a new pathway for pain management after rotator cuff surgery will reduce pain.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~post op days 1,2,7,14
This trial's timeline: 3 weeks for screening, Varies for treatment, and post op days 1,2,7,14 for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
- Worst NRS With Movement
Secondary outcome measures
Block Duration
Pain Score at Rest
Patient Satisfaction With Pain Management
+1 more

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: After GroupExperimental Treatment1 Intervention
We plan to have 70 patients studied after initiation of a pathway.
Group II: Before GroupActive Control1 Intervention
We plan to have 70 patients studied prior to initiation of a pathway.

Find a Location

Who is running the clinical trial?

Hospital for Special Surgery, New YorkLead Sponsor
243 Previous Clinical Trials
59,224 Total Patients Enrolled
2 Trials studying Shoulder Pain
182 Patients Enrolled for Shoulder Pain
Jacques YaDeauPrincipal InvestigatorHospital for Special Surgery, New York

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
Rotator Cuff Pathway
2018. "Rotator Cuff Pathway". ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT03717753.
~21 spots leftby Apr 2025
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