NonNarcotic Pain Control in Percutaneous Needle Tenotomy of Elbow

Part of paid clinical trials in Coral Springs, Florida.

Sponsor
The Cleveland Clinic
Study ID
NCT06373978
Phase
PHASE4
Status
Recruiting
Apply to this trial

Conditions

  • Chronic Pain
  • Elbow Pain

Eligibility Criteria

Sex
ALL
Age
18 Years - 65 Years
Healthy Volunteers
Not accepted

Interventions

  • Diclofenac — DRUG
    50mg every 8hours as needed for pain
  • Tramadol — DRUG
    50mg every 8hours as needed for pain
  • Acetaminophen — OTHER
    1000mg every 8hours as needed for pain

Study Details

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.

Key Dates

Start date
Aug 12, 2024
Status verified
Feb 2026
Primary completion
Jun 30, 2026
Completion
Jun 30, 2026

Study Design

Enrollment
92 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE

Arms

  • Active Comparator: Diclofenac
    50mg
  • Active Comparator: Tramadol
    50mg
  • Sham Comparator: Acetaminophen
    1000mg

Primary Outcome Measure

Number of pills taken [ Time Frame: 10 days ]

Central Contacts

Locations (2)

FacilityCityStateZIPSite coordinators
The Cleveland Clinic FloridaCoral SpringsFlorida33067
Erin Clancy, BA
[email protected]
216.970.6796
Jennifer Baldwin
[email protected]
216.390.5833
Michael Dakkak, DO (PRINCIPAL_INVESTIGATOR)
The Cleveland Clinic OhioAvonOhio44011
Jennifer Baldwin
[email protected]
216.390.5833
Jason Genin, DO (SUB_INVESTIGATOR)
Vikas Patel, DO (SUB_INVESTIGATOR)

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