A Randomized Controlled Trial: Alternative Post Procedural Analgesia With NSAIDs vs Opioids in Percutaneous Needle Tenotomy of Elbow

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Drug, Other
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

This study is a double-blind, randomized controlled trial comparing the effectiveness of oral acetaminophen, diclofenac, and tramadol in reducing the consumption of narcotic doses (primary outcome) and minimizing patients' exposure to narcotics (secondary outcome) following an ultrasound-guided percutaneous needle tenotomy procedure on the lateral elbow.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: f
View:

• Provision of signed and dated informed consent form

• Stated willingness to comply with all study procedures and availability for the duration of the study

• Male or female, aged 18-65 years

• Percutaneous Needle Tenotomy of Lateral Elbow Procedure

• Ability to take oral medication and willingness to participate in a 2-week follow-up pill counts

• Musculoskeletal ultrasound or MRI with diagnosis of tendinosis of the common extensor tendon of the elbow

Locations
United States
Florida
The Cleveland Clinic Florida
RECRUITING
Coral Springs
Ohio
The Cleveland Clinic Ohio
RECRUITING
Avon
Contact Information
Primary
Jennifer Baldwin
baldwij@ccf.org
216.390.5833
Backup
Alison Klika, MS
klikaa@ccf.org
216 444-4954
Time Frame
Start Date: 2024-08-12
Estimated Completion Date: 2025-12-15
Participants
Target number of participants: 92
Treatments
Active_comparator: Diclofenac
50mg
Active_comparator: Tramadol
50mg
Sham_comparator: Acetaminophen
1000mg
Related Therapeutic Areas
Sponsors
Leads: The Cleveland Clinic

This content was sourced from clinicaltrials.gov