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
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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