Gait Analysis and Neuromuscular Function After Primary Total Hip Replacement

NCT01229293 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 39

Last updated 2012-09-25

No results posted yet for this study

Summary

This study is conducted at Odense University Hospital(OUH) in collaboration with Institute of Clinical Biomechanics and Sport Science, University of Southern Denmark and Clinical Institute, University of Southern Denmark

Aim: To evaluate the effect of implant design on postoperative total leg muscle function recovery and gait in hip replacement patients.

Design: A prospective randomized controlled clinical trial where patients are randomized into (A) total hip arthroplasty surgery (THA) or (B) resurfacing total hip replacement surgery (RTHA). Pre-surgery assessment and follow-up will be conducted at 8, 26 and 52 wks post-surgery.

Conditions

Interventions

PROCEDURE

Articular Surface Replacement (ASR)

Articular surface replacement, DePuy, posterolateral approach used

PROCEDURE

Standard Total Hip Arthroplasty (THA)

Device: Biomet 28mm

Sponsors & Collaborators

  • Ministry of the Interior and Health, Denmark

    collaborator OTHER_GOV
  • The Danish Rheumatism Association

    collaborator OTHER
  • Odense University Hospital

    collaborator OTHER
  • University of Southern Denmark

    lead OTHER

Principal Investigators

  • Søren Overgaard, Prof., MD., PhD · Odense University Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
40 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-02-28
Primary Completion
2010-03-31
Completion
2011-11-30

Countries

  • Denmark

Study Locations

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Entities

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 NCT01229293 on ClinicalTrials.gov