NonNarcotic Pain Control in Percutaneous Needle Tenotomy of Elbow
Launched by THE CLEVELAND CLINIC · Apr 16, 2024
Trial Information
Current as of July 09, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is looking at different pain relief options for people who have elbow pain, specifically after a procedure called percutaneous needle tenotomy, which is done to treat a condition called tendinosis in the elbow. The study will compare three types of oral medications—acetaminophen, diclofenac, and tramadol—to see which one helps reduce the need for narcotic painkillers. The goal is to find a way to manage pain effectively while minimizing the use of stronger, addictive medications.
To participate in this study, you need to be between 18 and 65 years old and have a specific type of elbow pain diagnosed through an ultrasound or MRI. You must also be able to take oral medications and commit to following the study procedures for about two weeks. If you have had prior elbow surgery, certain medical conditions, or are taking other investigational drugs, you may not be eligible. Participants will be monitored for their pain levels and medication use, and everyone involved will be kept in the dark about which medication they are receiving to ensure fair results.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 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
- Exclusion Criteria:
- • • Any full thickness common extensor tendon tear of the elbow
- • Prior history of elbow surgery
- • Symptomatic cervical radiculopathy
- • Concurrent symptoms of the medial elbow
- • Treatment with another investigational drug or other intervention concurrently or previously that would interfere with postoperative pain control
- • Psychiatric illness that impedes evaluation of pain and/or narcotics use
- • No history of inflammatory arthritis, diabetes, chronic regional pain syndrome, connective tissue disease, fibromyalgia or autoimmune disease
- • No contraindications to NSAIDs or Opioids
About The Cleveland Clinic
The Cleveland Clinic is a renowned nonprofit academic medical center based in Cleveland, Ohio, recognized for its commitment to advancing healthcare through innovative research and clinical excellence. As a leading sponsor of clinical trials, the Cleveland Clinic leverages its multidisciplinary expertise and state-of-the-art facilities to conduct groundbreaking studies aimed at improving patient outcomes across a wide range of medical conditions. With a strong emphasis on patient-centered care, the institution fosters collaboration among researchers, clinicians, and patients to explore new treatments and therapies, contributing significantly to the global body of medical knowledge.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Coral Springs, Florida, United States
Avon, Ohio, United States
Patients applied
Trial Officials
Michael Dakkak, DO
Principal Investigator
Cleveland Clinic Florida
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported