A Retro/Prospective Multi-Centre Data Capture on REDAPT Sleeved Stem

NCT05600712 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 45

Last updated 2024-03-15

No results posted yet for this study

Summary

Retro/Prospective study to collect 2 year follow-up on REDAPT sleeved stem.

Conditions

  • Safety and Performance

Interventions

DEVICE

REDAPT Sleeved Stem

The REDAPT Sleeved Stem is designed to provide secondary proximal support to the distal fixation and enhance implant stability.

Sponsors & Collaborators

  • Smith & Nephew, Inc.

    collaborator INDUSTRY
  • Foundation for Orthopaedic Research and Education

    lead OTHER

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-01-11
Primary Completion
2024-02-14
Completion
2024-02-14
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05600712 on ClinicalTrials.gov