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NCT06323980 · ClinicalTrials.gov registry record · NA

INHANCE Stemless Reverse Shoulder IDE

A NA study of Arthroplasty and Shoulder, sponsored by DePuy Orthopaedics.

Recruiting
Registry status
NA
Development phase
168
Enrollment target
18
Study locations

NCT06323980 is a NA study of Arthroplasty and Shoulder that is actively recruiting participants, run by DePuy Orthopaedics. The registered enrollment target is 168 participants, below the 208-participant average among 5 other Arthroplasty trials with a reported enrollment target (19% lower). The trial reports 18 study locations across 12 states.

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The verdict

NCT06323980, a NA study of Arthroplasty and Shoulder, is actively recruiting participants, sponsored by DePuy Orthopaedics.

RECRUITING
Registry status
NA
Development phase
168 participants
Enrollment target
18
Study locations

Study Summary

2:1 Randomized, Controlled, Multi-Center, Prospective, Pre-Market Study of the INHANCE Stemless Reverse Cementless Total Shoulder.

Conditions Studied

Arthroplasty Shoulder Replacement

Interventions

  • DEVICE Reverse Total Shoulder

Study Locations (18)

Ohio

  • Crystal Clinic Orthopaedic Center - Akron
  • Lindner Research Center - Cincinnati
  • Cleveland Clinic - Cleveland

California

  • Hoag Orthopedic Institute - Irvine
  • Cedars Sinai Medical Center - Los Angeles

North Carolina

  • OrthoCarolina Research Institute Charlotte - Charlotte
  • Duke Orthopaedics of Raleigh - Raleigh

Pennsylvania

  • St. Luke's University Health Network - Bethlehem
  • Rothman Orthopaedics Institute - Philadelphia

Utah

  • TOSH- The Orthopedic Specialty Hospital - Murray
  • University of Utah - Salt Lake City

Florida

  • Orthopedic Center of Palm Beach County - Atlantis

Massachusetts

  • Boston Bone & Joint Institute BBJI Formerly BSSC - Waltham

Michigan

  • Trinity Health Grand Rapids - Grand Rapids

Trial Details

FieldValue
Enrollment Target 168 participants
Start Date 2025-03-04
Est. Completion 2028-09-29
Phase NA

Sponsor

DePuy Orthopaedics

38 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06323980

The ClinicalTrials.gov registry entry for NCT06323980 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 168 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 208-participant average among 5 other Arthroplasty trials with a reported enrollment target (19% lower). The listed sponsor is DePuy Orthopaedics, which has 38 total studies on file at ClinicalTrials.gov.

The record links to 3 conditions, with Arthroplasty appearing as the primary indexed condition, and to 1 intervention - of which Reverse Total Shoulder is the first listed.

NCT06323980 reports 18 study locations spanning 12 distinct geographic areas - top geographies include Ohio, California, North Carolina.

Frequently Asked Questions

What is clinical trial NCT06323980 about?

NCT06323980 is a clinical study titled "INHANCE Stemless Reverse Shoulder IDE". 2:1 Randomized, Controlled, Multi-Center, Prospective, Pre-Market Study of the INHANCE Stemless Reverse Cementless Total Shoulder.

What is the current status of trial NCT06323980?

This trial is currently recruiting. It is a NA study. The enrollment target is 168 participants. The study started on 2025-03-04. Estimated completion is 2028-09-29.

What conditions does trial NCT06323980 study?

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

What interventions are being tested in trial NCT06323980?

The interventions under investigation include: Reverse Total Shoulder (DEVICE).

Who is sponsoring clinical trial NCT06323980?

This trial is sponsored by DePuy Orthopaedics, which has 38 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06323980 being conducted?

This trial has 18 study locations across California, Florida, Massachusetts, Michigan, Missouri. 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.