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

Sponsor
Hospital Ambroise Paré Paris (Other)
Overall Status
Completed
CT.gov ID
NCT01520961
Collaborator
(none)
82
1
14
5.9

Study Details

Study Description

Brief Summary

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 or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    82 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Prospective
    Official Title:
    Approach Your Neck Fracture
    Study Start Date :
    Jan 1, 2012
    Actual Primary Completion Date :
    Mar 1, 2013
    Actual Study Completion Date :
    Mar 1, 2013

    Arms and Interventions

    Arm Intervention/Treatment
    Hueter Anterior Approach

    posterolateral approach

    Outcome Measures

    Primary Outcome Measures

    1. Measurement of mobility [Timed Get Up and Go Test at six weeks]

      Efficacity issue

    Secondary Outcome Measures

    1. Measurement of mobility [Using 2 cruches or walker at 6 weeks after surgery]

    2. Dislocation rate [At 6 weeks postoperatively]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Femoral Neck Fracture

    • Partial Hip Arthroplasty

    Exclusion Criteria:
    • Total Hip Arthroplasty

    • Osteosynthesis

    • Pathologic fracture

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Ambroise Paré Hospital. Orthopaedic surgery department Boulogne-Billancourt Ile de France France 92100

    Sponsors and Collaborators

    • Hospital Ambroise Paré Paris

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Shahnaz Klouche, MD, Physician Responsible of Clinical Research, Hospital Ambroise Paré Paris
    ClinicalTrials.gov Identifier:
    NCT01520961
    Other Study ID Numbers:
    • APR122011
    First Posted:
    Jan 30, 2012
    Last Update Posted:
    Feb 9, 2015
    Last Verified:
    Feb 1, 2015
    Keywords provided by Shahnaz Klouche, MD, Physician Responsible of Clinical Research, Hospital Ambroise Paré Paris
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Feb 9, 2015