Restoration of Leg Length, Offset, and Center of Rotation in Total Hip Replacement
Recruitment status was Recruiting
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Purpose
The investigators aim to demonstrate the ability to accurately measure and restore leg length, offset, and center of rotation during a total hip replacement through a new technique that uses the femoral component as a measurement tool. The operative technique requires inserting the femoral component prior to performing the femoral neck osteotomy. After the femoral component is implanted, a reference guide is attached to the femoral component and guides a screw into the ilium at a fixed distance from the femoral component. The pre-arthroplasty measurements of leg length and offset are recorded. The femoral neck osteotomy is performed, and the native femoral head is removed and measured. The acetabular socket is prepared and the acetabular component is inserted. A repeat measurement with trial modular neck components is taken and allows the surgeon an additional opportunity to accurately recreate leg length and offset with the final component. The reference screw is removed from the ilium and the incision is closed.
| Condition | Intervention |
|---|---|
|
Arthritis |
Procedure: Total hip replacement |
| Study Type: | Interventional |
| Study Design: | Allocation: Non-Randomized Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Restoration of Leg Length, Offset, and Center of Rotation in Total Hip Replacement |
- Leg Length and total offset [ Time Frame: 2 weeks ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 100 |
| Study Start Date: | June 2007 |
| Estimated Study Completion Date: | April 2010 |
| Estimated Primary Completion Date: | April 2009 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: 1
Leg Length and offset measurement arm
|
Procedure: Total hip replacement
Total hip replacement typically preformed for hip arthritis
Other Name: Measurement Arm
|
Show Detailed Description
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- Hip arthritis requiring a total hip replacement through a superior approach
Exclusion Criteria:
- Non-english speaking
- Need for a cemented femoral stem
- Acute femoral neck fracture
Contacts and Locations| Contact: William Kurtz, MD | 615-963-1437 | kurtzwb@tnortho.com |
| United States, Tennessee | |
| Baptist Hospital | Recruiting |
| Nashville, Tennessee, United States, 37203 | |
| Principal Investigator: | William B Kurtz, MD | Tennessee Orthopedic Alliance |
More Information
Additional Information:
Publications:
| Responsible Party: | William B Kurtz, Tennessee Orthopedic Alliance |
| ClinicalTrials.gov Identifier: | NCT00738803 History of Changes |
| Other Study ID Numbers: | 2615 |
| Study First Received: | August 18, 2008 |
| Last Updated: | February 5, 2009 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by Tennessee Orthopedic Alliance:
|
leg length hip arthroplasty offset |
Additional relevant MeSH terms:
|
Arthritis Joint Diseases Musculoskeletal Diseases |
ClinicalTrials.gov processed this record on May 19, 2013