NonNarcotic Pain Control in Percutaneous Needle Tenotomy of Elbow

NCT ID
NCT06373978
Registry status
Recruiting
Study type
Interventional
Phase
Phase 4
Sponsor
The Cleveland Clinic
Conditions
Chronic Pain, Elbow Pain

Overview

ClinicalTrials.gov lists this study as Recruiting.

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

Enrollment: 92 participants (Estimated).

What is being studied

  • Other: Acetaminophen
  • Intervention: Acetaminophen
  • Intervention: Acetanilides
  • Intervention: Acids, Carbocyclic
  • Intervention: Alcohols
  • Intervention: Amides
  • Intervention: Amines
  • Intervention: Anilides
  • Intervention: Aniline Compounds
  • Intervention: Carboxylic Acids
  • Intervention: Cyclohexanols
  • Drug: Diclofenac
  • Intervention: Diclofenac
  • Intervention: Dimethylamines
  • Intervention: Fatty Alcohols
  • Intervention: Hexanols
  • Intervention: Lipids
  • Intervention: Methylamines
  • Intervention: Organic Chemicals
  • Intervention: Phenylacetates
  • Drug: Tramadol
  • Intervention: Tramadol

Who may be eligible

Ages
18 Years to 65 Years
Sex
All
Healthy volunteers accepted
No

ClinicalTrials.gov lists the following 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

Study locations

2 study locations are listed.

Recruiting site status is explicitly provided for 2 locations; 2 are listed as Recruiting.

Countries: United States

  • Florida, United States: 1
  • Ohio, United States: 1

Sample of listed locations

  • The Cleveland Clinic Florida — Coral Springs, Florida, 33067, United States — Recruiting
  • The Cleveland Clinic Ohio — Avon, Ohio, 44011, United States — Recruiting

Study details

Start date
August 12, 2024
Primary completion date
June 30, 2027
Completion date
June 30, 2027
First posted
April 18, 2024

Source and update information

Source
ClinicalTrials.gov
NCT ID
NCT06373978
Registry last updated
August 28, 2026
QualifiedStudies registry data refreshed
October 2, 2026
QualifiedStudies record fetched
October 2, 2026

View NCT06373978 on ClinicalTrials.gov

Trial information can change. Confirm current study details with the study team or the registry.

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