Functional Recovery After Partial Hip Arthroplasty: Anterior or Posterolateral Approach? (AYNF)

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Shahnaz Klouche, MD, Hôpital Ambroise Paré
ClinicalTrials.gov Identifier:
NCT01520961
First received: January 19, 2012
Last updated: November 14, 2013
Last verified: November 2013
  Purpose

Hueter anterior approach as described by Siguier allows an anatomical approach without muscle or tendon sections. It minimizes the rate of dislocation after primary total hip arthroplasty (1.5%, Sariali)and seems to allow quicker rehabilitation.

The investigators hypothesis was Hueter anterior approach allows quicker functional recovery after partial hip replacement.


Condition
Hip Arthroplasty
Femoral Neck Fractures

Study Type: Observational
Study Design: Observational Model: Case Control
Time Perspective: Prospective
Official Title: Approach Your Neck Fracture

Resource links provided by NLM:


Further study details as provided by Hôpital Européen Marseille:

Primary Outcome Measures:
  • Measurement of mobility [ Time Frame: Timed Get Up and Go Test at six weeks ] [ Designated as safety issue: No ]
    Efficacity issue


Secondary Outcome Measures:
  • Measurement of mobility [ Time Frame: Using 2 cruches or walker at 6 weeks after surgery ] [ Designated as safety issue: No ]
  • Dislocation rate [ Time Frame: At 6 weeks postoperatively ] [ Designated as safety issue: Yes ]

Enrollment: 82
Study Start Date: January 2012
Study Completion Date: March 2013
Primary Completion Date: March 2013 (Final data collection date for primary outcome measure)
Groups/Cohorts
Hueter Anterior Approach
posterolateral approach

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

Partial Hip Arthroplasty for Femoral Neck Fracture

Criteria

Inclusion Criteria:

  • Femoral Neck Fracture
  • Partial Hip Arthroplasty

Exclusion Criteria:

  • Total Hip Arthroplasty
  • Osteosynthesis
  • Pathologic fracture
  Contacts and Locations
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Please refer to this study by its ClinicalTrials.gov identifier: NCT01520961

Locations
France
Ambroise Paré Hospital. Orthopaedic surgery department
Boulogne-Billancourt, Ile de France, France, 92100
Sponsors and Collaborators
Hôpital Européen Marseille
  More Information

No publications provided

Responsible Party: Shahnaz Klouche, MD, Physician Responsible of Clinical Research, Hôpital Ambroise Paré
ClinicalTrials.gov Identifier: NCT01520961     History of Changes
Other Study ID Numbers: APR122011
Study First Received: January 19, 2012
Last Updated: November 14, 2013
Health Authority: France: French Agency of Sanitary Safety of the Products of Health

Keywords provided by Hôpital Européen Marseille:
Partial Hip Arthroplasty

Additional relevant MeSH terms:
Femoral Neck Fractures
Fractures, Bone
Femoral Fractures
Hip Fractures
Leg Injuries
Wounds and Injuries

ClinicalTrials.gov processed this record on October 23, 2014