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NCT02811003 · ClinicalTrials.gov registry record · NA

Achilles Tendon Repair With Bioinductive Implant

A NA study of Tendinopathy, sponsored by Smith & Nephew.

Completed
Registry status
NA
Development phase
20
Enrollment target
2
Study locations

NCT02811003 is a NA study of Tendinopathy that has completed, run by Smith & Nephew. The registered enrollment target is 20 participants, below the 1,065-participant average among 10 other Tendinopathy trials with a reported enrollment target (98% lower). The trial reports 2 study locations across 2 states.

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The verdict

NCT02811003, a NA study of Tendinopathy, has completed, sponsored by Smith & Nephew.

COMPLETED
Registry status
NA
Development phase
20 participants
Enrollment target
2
Study locations

Study Summary

To evaluate bioinduction of new tissue and tendon healing after implantation of the Rotation Medical Bioinductive Implant used as adjunct to surgical repair in the treatment of insertional Achilles tendonitis.

Conditions Studied

Tendinopathy

Interventions

  • DEVICE Rotation Medical Bioinductive Implant

Study Locations (2)

Maryland

  • MedStar Union Memorial Hospital - Baltimore

Pennsylvania

  • Allegheny Health Network - Pittsburgh

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2016-06-03
Est. Completion 2019-09-17
Phase NA

Sponsor

Smith & Nephew

72 total trials

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What the Registry Record Tells You About NCT02811003

The ClinicalTrials.gov registry entry for NCT02811003 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 1,065-participant average among 10 other Tendinopathy trials with a reported enrollment target (98% lower). The listed sponsor is Smith & Nephew, which has 72 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Tendinopathy appearing as the primary indexed condition, and to 1 intervention - of which Rotation Medical Bioinductive Implant is the first listed.

NCT02811003 reports 2 study locations spanning 2 distinct geographic areas - top geographies include Maryland, Pennsylvania.

Frequently Asked Questions

What is clinical trial NCT02811003 about?

NCT02811003 is a clinical study titled "Achilles Tendon Repair With Bioinductive Implant". To evaluate bioinduction of new tissue and tendon healing after implantation of the Rotation Medical Bioinductive Implant used as adjunct to surgical repair in the treatment of insertional Achilles tendonitis.

What is the current status of trial NCT02811003?

This trial is currently completed. It is a NA study. The enrollment target is 20 participants. The study started on 2016-06-03. Estimated completion is 2019-09-17.

What conditions does trial NCT02811003 study?

This clinical trial studies the following conditions: Tendinopathy.

What interventions are being tested in trial NCT02811003?

The interventions under investigation include: Rotation Medical Bioinductive Implant (DEVICE).

Who is sponsoring clinical trial NCT02811003?

This trial is sponsored by Smith & Nephew, which has 72 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02811003 being conducted?

This trial has 2 study locations across Maryland, Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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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.