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

NCT03234192 · ClinicalTrials.gov registry record · NA

Effectiveness of the Astym Technique, the Graston Technique, and Therapeutic Ultrasound in the Treatment of Lateral Epicondylosis.

A NA study, sponsored by NYU Langone Health.

Terminated
Registry status
NA
Development phase
21
Enrollment target

NCT03234192: Clinical Trial NA study, sponsored by NYU Langone Health.

NCT03234192 is a NA study that was terminated before completion, run by NYU Langone Health. The registered enrollment target is 21 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT03234192, a NA study, was terminated before completion, sponsored by NYU Langone Health.

TERMINATED
Registry status
NA
Development phase
21 participants
Enrollment target

Study Summary

The purpose of this study is to examine the effectiveness of three common techniques for the treatment of lateral epicondylosis. Through objective and subjective assessments this study will determine the effectiveness of the Astym Treatment Technique, the Graston Treatment Technique, and therapeutic ultrasound in the conservative treatment of lateral epicondylosis. It is hypothesized that the more manual Astym technique and Graston technique will produce more significant results than the more frequently utilized ultrasound.

Primary Outcome

This is a 15 item self-reported questionnaire to measure perceived pain and disability in people with Lateral Epicondylosis (LE)

Interventions

  • PROCEDURE Therapeutic ultra sound
  • PROCEDURE Astym Treatment Technique
  • PROCEDURE Graston Treatment Technique

Trial Details

FieldValue
Enrollment Target 21 participants
Start Date 2017-06-10
Est. Completion 2019-05-23
Phase NA
NYU Langone Health

1,164 total trials

Why NCT03234192 stopped before completion

NCT03234192 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 21 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).

The record links to 0 conditions, and to 3 interventions - of which Therapeutic ultra sound is the first listed.

NCT03234192 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03234192 about?

NCT03234192 is a clinical study titled "Effectiveness of the Astym Technique, the Graston Technique, and Therapeutic Ultrasound in the Treatment of Lateral Epicondylosis.". The purpose of this study is to examine the effectiveness of three common techniques for the treatment of lateral epicondylosis. Through objective and subjective assessments this study will determine the effectiveness of the Astym Treatment Technique, the Graston Treatment Technique, and therapeutic...

What is the current status of trial NCT03234192?

This trial is currently terminated. It is a NA study. The enrollment target is 21 participants. The study started on 2017-06-10. Estimated completion is 2019-05-23.

What interventions are being tested in trial NCT03234192?

The interventions under investigation include: Therapeutic ultra sound (PROCEDURE), Astym Treatment Technique (PROCEDURE), Graston Treatment Technique (PROCEDURE).

Who is sponsoring clinical trial NCT03234192?

This trial is sponsored by NYU Langone Health, which has 1,164 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03234192's enrollment target sits among peer trials

21 1762nd of 2000 higher than 233 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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

  • NCT02447874 · 21 participants · Phase 1

    Arginine Therapy for the Treatment of Pain in Children With Sickle Cell Disease

  • NCT03826992 · 21 participants · Phase 1

    Venetoclax Combined With Vyxeos (CPX-351) for Participants With Relapsed or Refractory Acute Leukemia

  • NCT04107077 · 21 participants · Phase 2

    Phase II Study of the Effects of Laparoscopic Hyperthermic Intraperitoneal Chemotherapy (HIPEC) in Patients With Advanced Gastric Cancer

  • NCT04158635 · 21 participants · Phase 1

    Gemcitabine, Nab-Paclitaxel, and Bosentan for the Treatment of Unresectable Pancreatic Cancer

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT03234192, the US trial registry maintained by the National Library of Medicine. NCT03234192 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.