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NCT00881998 Clinical Trial

Study of Two Surgical Approaches for Total Hip Arthroplasty

Total Hip Arthroplasty Clinical Trial

Official title:
Prospective, Randomized Study of Two Surgical Approaches for Total Hip Arthroplasty

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00881998
Other study ID # RIUWHOZ-09-02
Secondary ID
Status Completed
Phase N/A
First received April 14, 2009
Last updated April 15, 2009

Study information
Verified date April 2009
Source Rothman Institute Orthopaedics
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

A prospective, comparative, randomized single surgeon study comparing minimally invasive total hip arthroplasty (MIS) via anterior approach to conventional total hip arthroplasty via anterolateral transgluteal approach.

Recruitment information / eligibility
Status Completed
Enrollment 100
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Patients diagnosed with osteoarthritis of the hip and have decided to undergo total hip arthroplasty

- Patients willing to sign the consent form

Exclusion Criteria:

- Patient is unwilling to sign the consent form

- Patient is involved in another study

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Procedure:
• Minimally Invasive Total Hip Arthroplasty

• Conventional Total Hip Arthroplasty

Locations
Country Name City State
United States Rothman Institute Orthorpaedics Philadelphia Pennsylvania

Sponsors (1)
Lead Sponsor Collaborator
Rothman Institute Orthopaedics

Country where clinical trial is conducted

United States, 

See also
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Withdrawn NCT01380665 - Prevena™ Incision Management System Over Primarily Closed Hip and Knee Incisions in Patients Immediately Post Total Hip and Knee Arthroplasty Phase 4
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