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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01520961
Other study ID # APR122011
Secondary ID
Status Completed
Phase N/A
First received January 19, 2012
Last updated February 6, 2015
Start date January 2012
Est. completion date March 2013

Study information

Verified date February 2015
Source Hospital Ambroise Paré Paris
Contact n/a
Is FDA regulated No
Health authority France: French Agency of Sanitary Safety of the Products of Health
Study type Observational

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 82
Est. completion date March 2013
Est. primary completion date March 2013
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Femoral Neck Fracture

- Partial Hip Arthroplasty

Exclusion Criteria:

- Total Hip Arthroplasty

- Osteosynthesis

- Pathologic fracture

Study Design

Observational Model: Case Control, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
France Ambroise Paré Hospital. Orthopaedic surgery department Boulogne-Billancourt Ile de France

Sponsors (1)

Lead Sponsor Collaborator
Hospital Ambroise Paré Paris

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Measurement of mobility Efficacity issue Timed Get Up and Go Test at six weeks No
Secondary Measurement of mobility Using 2 cruches or walker at 6 weeks after surgery No
Secondary Dislocation rate At 6 weeks postoperatively Yes
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