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

NCT04050748 · ClinicalTrials.gov registry record · NA

Achilles Tendon Lengthening With Traditional vs. Accelerated Rehab

A NA study of Achilles Tendon Rupture, sponsored by Henry Ford Health System.

Completed
Registry status
NA
Development phase
18
Enrollment target
1
Study location

NCT04050748 is a NA study of Achilles Tendon Rupture that has completed, run by Henry Ford Health System. The registered enrollment target is 18 participants. The trial reports 1 study location across 1 state.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT04050748, a NA study of Achilles Tendon Rupture, has completed, sponsored by Henry Ford Health System.

COMPLETED
Registry status
NA
Development phase
18 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to evaluate the surgically repaired tendon of a ruptured achilles tendon. We will investigate fixation slippage and tendon creep and correlate how these post-repair findings can contribute to outcomes of tendon repairs.

Conditions Studied

Interventions

  • PROCEDURE Achilles tendon repair

Study Locations (1)

Michigan

  • Health Ford Health System - Detroit

Trial Details

FieldValue
Enrollment Target 18 participants
Start Date 2017-06-01
Est. Completion 2019-06-05
Phase NA

Sponsor

Henry Ford Health System

234 total trials

What the Registry Record Tells You About NCT04050748

The ClinicalTrials.gov registry entry for NCT04050748 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 18 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Henry Ford Health System, which has 234 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Achilles Tendon Rupture appearing as the primary indexed condition, and to 1 intervention - of which Achilles tendon repair is the first listed.

NCT04050748 reports 1 study location spanning 1 distinct geographic area - top geographies include Michigan.

Frequently Asked Questions

What is clinical trial NCT04050748 about?

NCT04050748 is a clinical study titled "Achilles Tendon Lengthening With Traditional vs. Accelerated Rehab". The purpose of this study is to evaluate the surgically repaired tendon of a ruptured achilles tendon. We will investigate fixation slippage and tendon creep and correlate how these post-repair findings can contribute to outcomes of tendon repairs.

What is the current status of trial NCT04050748?

This trial is currently completed. It is a NA study. The enrollment target is 18 participants. The study started on 2017-06-01. Estimated completion is 2019-06-05.

What conditions does trial NCT04050748 study?

This clinical trial studies the following conditions: Achilles Tendon Rupture.

What interventions are being tested in trial NCT04050748?

The interventions under investigation include: Achilles tendon repair (PROCEDURE).

Who is sponsoring clinical trial NCT04050748?

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

Where is trial NCT04050748 being conducted?

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

Similar trials for Achilles Tendon Rupture

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.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.