Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00257634 · ClinicalTrials.gov registry record · Phase 3

Randomized Trial of Iontophoresis Versus Injection of Corticosteroids for Lateral Epicondylitis

A Phase 3 study of Lateral Epicondylitis and Work-related Injury, sponsored by Henry Ford Health System.

Completed
Registry status
Phase 3
Development phase
80
Enrollment target
1
Study location

NCT00257634: Completed Phase 3 study of Lateral Epicondylitis and Work-related Injury, sponsored by Henry Ford Health System.

NCT00257634 is a Phase 3 study of Lateral Epicondylitis and Work-related Injury that has completed, run by Henry Ford Health System. The registered enrollment target is 80 participants, below the 116-participant average among 7 other Lateral Epicondylitis trials with a reported enrollment target (31% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00257634, a Phase 3 study of Lateral Epicondylitis and Work-related Injury, has completed, sponsored by Henry Ford Health System.

COMPLETED
Registry status
Phase 3
Development phase
80 participants
Enrollment target
1
Study location

Study Summary

The purpose of this project is to compare different treatment options for lateral epicondylitis. Lateral epicondylitis is a pain condition involving extensor muscles fo the forearm originating from the lateral epicondyle. Controversy exists regarding the method of delivering pain relief so that conditioning and strengthening can be initiated and progress appropriately. Our hypothesis is that the steady even delivery via iontophoresis (compared to injection will provide better pain control and allow physical therapy to progress more effectively.

Interventions

  • DRUG dexamethasone to injury site

Study Locations (1)

Michigan

  • Henry Ford Health System - Detroit

Trial Details

FieldValue
Enrollment Target 80 participants
Start Date 2004-12
Est. Completion 2007-01
Phase Phase 3
Henry Ford Health System

234 total trials

What the finished NCT00257634 record still lists

NCT00257634 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 80 participants, a relatively small participant target, below the 116-participant average among 7 other Lateral Epicondylitis trials with a reported enrollment target (31% lower).

The record links to 2 conditions, with Lateral Epicondylitis appearing as the primary indexed condition, and to 1 intervention - of which dexamethasone to injury site is the first listed.

NCT00257634 reports a single indexed study location in Michigan.

Frequently Asked Questions

What is clinical trial NCT00257634 about?

NCT00257634 is a clinical study titled "Randomized Trial of Iontophoresis Versus Injection of Corticosteroids for Lateral Epicondylitis". The purpose of this project is to compare different treatment options for lateral epicondylitis. Lateral epicondylitis is a pain condition involving extensor muscles fo the forearm originating from the lateral epicondyle. Controversy exists regarding the method of delivering pain relief so that cond...

What is the current status of trial NCT00257634?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 80 participants. The study started on 2004-12. Estimated completion is 2007-01.

What conditions does trial NCT00257634 study?

This clinical trial studies the following conditions: Lateral Epicondylitis, Work-related Injury.

What interventions are being tested in trial NCT00257634?

The interventions under investigation include: dexamethasone to injury site (DRUG).

Who is sponsoring clinical trial NCT00257634?

This trial is sponsored by Henry Ford Health System, which has 234 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00257634 being conducted?

This trial has 1 study location across Michigan. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Lateral Epicondylitis

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT01243931 · 80 participants · NA

    Optical Coherence Tomography Guided Transepithelial Phototherapeutic Keratectomy

  • NCT01659203 · 80 participants · Phase 1

    Proton or Photon RT for Retroperitoneal Sarcomas

  • NCT01803451 · 80 participants · Early Phase 1

    Glucagon-like Peptide 1, Glucose Metabolism and Gastric Bypass

  • NCT01964859 · 80 participants · Phase 2

    Feasibility Study for Fibroblast Autologous Skin Grafts

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00257634, the US trial registry maintained by the National Library of Medicine. NCT00257634 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.