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NCT04861714 · ClinicalTrials.gov registry record · NA

Evaluation of Regeneten Augmentation for Subscapularis Healing After Total Shoulder Arthroplasty (RESTOR)

A NA study of Arthroplasty, Replacement, Shoulder, sponsored by Ohio State University.

Active
Registry status
NA
Development phase
75
Enrollment target
1
Study location

NCT04861714 is a NA study of Arthroplasty, Replacement, Shoulder that is active but no longer recruiting, run by Ohio State University. The registered enrollment target is 75 participants. The trial reports 1 study location across 1 state.

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The verdict

NCT04861714, a NA study of Arthroplasty, Replacement, Shoulder, is active but no longer recruiting, sponsored by Ohio State University.

ACTIVE NOT RECRUITING
Registry status
NA
Development phase
75 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to evaluate whether augmentation of subscapularis repair with the Regeneten implant after anatomic total shoulder arthroplasty (TSA) can improve rates of subscapularis healing and improve clinical outcomes.

Interventions

  • DEVICE Regeneten
  • PROCEDURE Standard repair

Study Locations (1)

Ohio

  • The Ohio State University Sports Medicine Center - Columbus

Trial Details

FieldValue
Enrollment Target 75 participants
Start Date 2020-07-14
Est. Completion 2027-04
Phase NA

Sponsor

Ohio State University

552 total trials

What the Registry Record Tells You About NCT04861714

The ClinicalTrials.gov registry entry for NCT04861714 describes a study currently listed as active not recruiting, categorized as NA. The registered enrollment target is 75 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Ohio State University, which has 552 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Arthroplasty, Replacement, Shoulder appearing as the primary indexed condition, and to 2 interventions - of which Regeneten is the first listed.

NCT04861714 reports 1 study location spanning 1 distinct geographic area - top geographies include Ohio.

Frequently Asked Questions

What is clinical trial NCT04861714 about?

NCT04861714 is a clinical study titled "Evaluation of Regeneten Augmentation for Subscapularis Healing After Total Shoulder Arthroplasty (RESTOR)". The purpose of this study is to evaluate whether augmentation of subscapularis repair with the Regeneten implant after anatomic total shoulder arthroplasty (TSA) can improve rates of subscapularis healing and improve clinical outcomes.

What is the current status of trial NCT04861714?

This trial is currently active not recruiting. It is a NA study. The enrollment target is 75 participants. The study started on 2020-07-14. Estimated completion is 2027-04.

What conditions does trial NCT04861714 study?

This clinical trial studies the following conditions: Arthroplasty, Replacement, Shoulder.

What interventions are being tested in trial NCT04861714?

The interventions under investigation include: Regeneten (DEVICE), Standard repair (PROCEDURE).

Who is sponsoring clinical trial NCT04861714?

This trial is sponsored by Ohio State University, which has 552 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04861714 being conducted?

This trial has 1 study location across Ohio. 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

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