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

This study is currently recruiting participants.
Verified February 2012 by Hôpital Ambroise Paré
Sponsor:
Information provided by (Responsible Party):
Shahnaz Klouche, MD, Hôpital Ambroise Paré
ClinicalTrials.gov Identifier:
NCT01520961
First received: January 19, 2012
Last updated: February 2, 2012
Last verified: February 2012
History of Changes
  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:

MedlinePlus related topics: Fractures
U.S. FDA Resources

Further study details as provided by Hôpital Ambroise Paré:

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:
  • Organic Brain Deficit [ Time Frame: Short Portable Mental Status Questionnaire preoperatively, at six weeks and three months after surgery ] [ Designated as safety issue: No ]
  • Quality of Life [ Time Frame: EQ-5D : Health-related quality of life preoperatively, at six weeks and three months after surgery ] [ Designated as safety issue: No ]
  • Routine activities [ Time Frame: ADL : Activity of Daily Living at six weeks and three months after surgery ] [ Designated as safety issue: No ]
  • Measurement of mobility [ Time Frame: Timed Get Up and Go Test at three months after surgery ] [ Designated as safety issue: No ]

Estimated Enrollment: 60
Study Start Date: December 2011
Estimated Study Completion Date: May 2012
Estimated Primary Completion Date: March 2012 (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
Please refer to this study by its ClinicalTrials.gov identifier: NCT01520961

Locations
France
Ambroise Paré Hospital. Orthopaedic surgery department Recruiting
Boulogne-Billancourt, Ile de France, France, 92100
Contact: Shahnaz Klouche, MD     + 33 6 28 35 04 78     klouche_shahnaz@yahoo.fr    
Principal Investigator: Philippe Hardy, Ph.D            
Sub-Investigator: Jean Langlois, MD            
Sponsors and Collaborators
Hôpital Ambroise Paré
  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: February 2, 2012
Health Authority: France: French Agency of Sanitary Safety of the Products of Health

Keywords provided by Hôpital Ambroise Paré:
Partial Hip Arthroplasty

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

ClinicalTrials.gov processed this record on May 23, 2013