# A Multicenter, Post-Market Clinical Follow-up Study of Subjects With the REDAPT™ System Monolithic Sleeveless/Sleeved Stem and/or Fully Porous Acetabular Shell With XLPE Liner and/or Modular Shell Components Previously Implanted

> **NCT03610789** · — · ENROLLING_BY_INVITATION · sponsor: **Smith & Nephew, Inc.** · enrollment: 220 (estimated)

## Conditions studied

- Hip Replacement

## Interventions

- **DEVICE:** REDAPT

## Key facts

- **NCT ID:** NCT03610789
- **Lead sponsor:** Smith & Nephew, Inc.
- **Sponsor class:** INDUSTRY
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** ENROLLING_BY_INVITATION
- **Start date:** 2018-05-07
- **Primary completion:** 2034-07-01
- **Final completion:** 2034-07-01
- **Target enrollment:** 220 (ESTIMATED)
- **Last updated:** 2025-01-06


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT03610789

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT03610789, "A Multicenter, Post-Market Clinical Follow-up Study of Subjects With the REDAPT™ System Monolithic Sleeveless/Sleeved Stem and/or Fully Porous Acetabular Shell With XLPE Liner and/or Modular Shell Components Previously Implanted". Retrieved via AI Analytics 2026-06-09 from https://api.ai-analytics.org/clinical/NCT03610789. Licensed CC0.

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*[Clinical trials dataset](/datasets/clinical-trials) · CC0 1.0*