Osteoarthritis, Hip Clinical Trial
Official title:
Comparing On-Table vs Off-Table Total Hip Arthroplasty Via the Direct Anterior Approach: A Prospective Randomized Trial
Verified date | February 2024 |
Source | Carilion Clinic |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The Direct Anterior Approach (DAA) is a common way to perform total hip arthroplasty. There are two main techniques to perform total hip replacement through the anterior approach. The first method is the "on-table" method, which uses a specialized surgical table, called a traction table. This table involves placing both feet in specialized boots that are then hooked up to the table, and allows for positioning of the operative leg with aid of the table. The major limitations associated with the traction table are the need for two additional staff members and the purchase of said table. The second method is the "off-table" method. In this method the patient is placed on a standard operating room table and the operative leg is manually positioned by the surgeon during the procedure . This obviates the need for the additional staff members or purchase of a specialized table. Both the "on-table" and "off-table" techniques are routinely used both worldwide and by our joint replacement specialists at Carilion Clinic. This study will aim to compare the efficiency and efficacy of performing the DAA for total hip arthroplasty utilizing either the "on-table" or "off- table" technique. Patients will be randomized to receive their total hip arthroplasty with either the "on- table" or "off-table" method.
Status | Active, not recruiting |
Enrollment | 93 |
Est. completion date | January 25, 2025 |
Est. primary completion date | January 25, 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - All patients undergoing primary unilateral THA - Patient 18 years of age and older - Patients who are able to provide consent Exclusion Criteria: - Bilateral procedure - Non-Primary arthroplasty - Prior non-arthroplasty operation requiring removal of hardware - Inability to have spinal anesthesia (blood thinners) - BMI > 40 - Active Smoking - HbA1c > 8.0 - Failure to meet medical clearance - Pregnant women per standard of care |
Country | Name | City | State |
---|---|---|---|
United States | Carilion Institute for Orthopaedics & Neurosciences | Roanoke | Virginia |
Lead Sponsor | Collaborator |
---|---|
Carilion Clinic | Virginia Tech Carilion School of Medicine and Research Institute |
United States,
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Cohen EM, Vaughn JJ, Ritterman SA, Eisenson DL, Rubin LE. Intraoperative Femur Fracture Risk During Primary Direct Anterior Approach Cementless Total Hip Arthroplasty With and Without a Fracture Table. J Arthroplasty. 2017 Sep;32(9):2847-2851. doi: 10.1016/j.arth.2017.04.020. Epub 2017 Apr 21. — View Citation
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Tian S, Goswami K, Manrique J, Blevins K, Azboy I, Hozack WJ. Direct Anterior Approach Total Hip Arthroplasty Using a Morphometrically Optimized Femoral Stem, a Conventional Operating Table, Without Fluoroscopy. J Arthroplasty. 2019 Feb;34(2):327-332. doi: 10.1016/j.arth.2018.10.023. Epub 2018 Oct 26. — View Citation
* Note: There are 11 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Set Up Time | Time point that patient enters room to time point of first incision | Time point that patient enters room to time point of first incision | |
Primary | Surgery Time | Time point of first incision to time point of dress application | Time point of first incision to time point of dress application | |
Primary | Takedown Time | Time point of Dress application to Time point of exiting operating room | Time point of Dress application to Time point of exiting operating room | |
Primary | Total Room Time | Time point that patient enters room to time point of exiting operating room | Time point that patient enters room to time point of exiting operating room | |
Secondary | Patient Reported Outcomes Measurement Information System/Hip Disability and Osteoarthritis Outcome Score, Joint Replacement scores | Hip pain measure survey on a scale of 0 - 10 with 0 = no pain and 10 = extreme pain | pre-op, 2 weeks post-op, 6 weeks post op, 1 year post op | |
Secondary | Visual Analog Scale scores | Hip, knee, ankle pain measure survey on a scale of 0 - 10 with 0 = no pain and 10 = worst pain | pre-op, 2 weeks post-op, 6 weeks post op, 1 year post op | |
Secondary | Narcotic Utillization | Measured by pill count usage and converted into MME | 2 weeks post op pill count |
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