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CompletedNCT00758355Updated Feb 23, 2017

Data Collection on ReCap/Magnum in Total Hip Replacement and Resurfacing

An observational study in Total Hip Resurfacing, sponsored by Zimmer Biomet. Completed at 6 sites in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2017-02-23.

Sponsored by Zimmer Biomet · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
150
Ages
18 Years and older
Sex
All
01

Study summary

Observational study on ReCap/Magnum in Total Hip Replacement and Resurfacing.

Read the detailed description

This observational study intends to collect efficacy and safety data on ReCap/Magnum in Total Hip Replacement and Resurfacing.

02

Conditions studied

  • Total Hip Resurfacing
03

In context

Lead sponsor

Zimmer Biomet is the lead sponsor of 271 studies on the registry; 28 are open to participants now.

Of its 23 completed or terminated interventional studies of FDA-regulated products, 19 (83%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Consecutive series of patients received Total Hip Replacement or Resurfacing with ReCap/Magnum for Their Respective Indications for Use/Intended Uses

Eligibility criteria

Inclusion Criteria:

Consecutive series of patients received Total Hip Replacement or Resurfacing with ReCap/Magnum for Its Respective Indications for Use/Intended Uses

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
150 participants (actual)
Patient registry
No

Groups and cohorts

  • M2A magnum

    Consecutive series of patients received Total Hip Resurfacing with ReCap/Magnum

  • Recap Magnum

    Consecutive series of patients received Total Hip Replacement with ReCap/Magnum

06

What researchers measure

Primary outcomes

  1. Postel-Merle d'Aubigné (PMA), Harris Hip Score

    Time frame: 1yr and 2yr

Secondary outcomes

  1. Complication

    Time frame: Any time

  2. Survival

    Time frame: 1yr and 2yr

07

Study locations

6 sites
  • CHU Amiens
    Amiens, 80000, France
  • CHU Pellegrin Tripode
    Bordeaux, France
  • CHU Hôpital Sud
    Grenoble, France
  • Polyclinique de Hénin Beaumont
    Henin-beaumont, France
  • Polyclinique de Riaumont
    Lievin, France
  • Clinique Saint Andre
    Reims, France
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 23, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00758355
Lead sponsor
Zimmer Biomet
Collaborators
Biomet France SARL
Responsible party
Sponsor
First posted
Sep 25, 2008
Start date
Mar 2008
Primary completion
Dec 2013
Completion
Jun 2016
Last update
Feb 23, 2017

Study contacts

Dominique Saragaglia, Pr
principal investigator · Hopital Sud - Echirolles

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2017. You cannot join it, but the record below documents what was studied.

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