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Completed No phase listed Observational

Depuy Synthes Lower Extremity Shaft Nail Registry

ClinicalTrials.gov ID: NCT05272631

Public ClinicalTrials.gov record NCT05272631. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 8:48 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Depuy Synthes Lower Extremity Shaft Nail Registry (RFN-Advanced™ Retrograde Femoral Nailing System/ TN-Advanced™ Tibial Nailing System)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this post-market registry is to monitor the clinical safety and performance (union rates and time to union) of two DePuy Synthes lower extremity shaft nails: RFN-Advanced Retrograde Femoral Nailing System (RFNA) and TN-Advanced Tibial Nailing System (TNA) in participants who have experienced femoral or tibial fractures, respectively, requiring fixation and stabilization or who require a revision due to a malunion or a nonunion.

Study identification

NCT ID
NCT05272631
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
DePuy Synthes Products, Inc.
Industry
Enrollment
241 participants

Conditions and interventions

Eligibility (public fields only)

Age range
12 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 4, 2022 (Actual)
Primary completion
Oct 31, 2025 (Actual)
Completion
Oct 31, 2025 (Actual)
Last update posted
Jan 16, 2026

2022 – 2025

United States locations

U.S. sites
8
U.S. states
7
U.S. cities
8
Facility City State ZIP Site status
Orthopedic Research Foundation, Inc Indianapolis Indiana 46278 —
Michigan Medicine; University of Michigan Ann Arbor Michigan 48109 —
University of Missouri Columbia Missouri 65211 —
Duke University Durham North Carolina 27705 —
Wake Forest Baptist Health Winston-Salem North Carolina 27157 —
Oregon Health and Science University Portland Oregon 97239 —
Vanderbilt University Medical Center Nashville Tennessee 37232 —
JPS Health Network Fort Worth Texas 76104 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05272631, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 16, 2026 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05272631 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →