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
- Measurement of mobility [Timed Get Up and Go Test at six weeks]
Efficacity issue
Secondary Outcome Measures
- Measurement of mobility [Using 2 cruches or walker at 6 weeks after surgery]
- 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: