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

NCT01025037 · ClinicalTrials.gov registry record · NA

Outcomes in Rotator Cuff Repair Using Graft Reinforcement

A NA study, sponsored by Stryker Trauma and Extremities.

Completed
Registry status
NA
Development phase
61
Enrollment target

NCT01025037 is a NA study that has completed, run by Stryker Trauma and Extremities. The registered enrollment target is 61 participants.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01025037, a NA study, has completed, sponsored by Stryker Trauma and Extremities.

COMPLETED
Registry status
NA
Development phase
61 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate patient shoulder functional outcomes following rotator cuff repairs reinforced with a surgical mesh.

Interventions

  • DEVICE Conexa Reconstructive Tissue Matrix

Trial Details

FieldValue
Enrollment Target 61 participants
Start Date 2009-10
Est. Completion 2014-04
Phase NA

Sponsor

Stryker Trauma and Extremities

30 total trials

What the Registry Record Tells You About NCT01025037

The ClinicalTrials.gov registry entry for NCT01025037 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 61 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Stryker Trauma and Extremities, which has 30 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Conexa Reconstructive Tissue Matrix is the first listed.

NCT01025037 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01025037 about?

NCT01025037 is a clinical study titled "Outcomes in Rotator Cuff Repair Using Graft Reinforcement". The purpose of this study is to evaluate patient shoulder functional outcomes following rotator cuff repairs reinforced with a surgical mesh.

What is the current status of trial NCT01025037?

This trial is currently completed. It is a NA study. The enrollment target is 61 participants. The study started on 2009-10. Estimated completion is 2014-04.

What interventions are being tested in trial NCT01025037?

The interventions under investigation include: Conexa Reconstructive Tissue Matrix (DEVICE).

Who is sponsoring clinical trial NCT01025037?

This trial is sponsored by Stryker Trauma and Extremities, which has 30 total clinical trials registered on ClinicalTrials.gov.

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.