Variability in Spinopelvic Parameters Among Patients Undergoing Total Hip Arthroplasty
Not Applicable
- Conditions
- Osteoarthritis, Hip
- Interventions
- Diagnostic Test: EOS X-Ray
- Registration Number
- NCT05212090
- Lead Sponsor
- Mayo Clinic
- Brief Summary
This research is being conducted to assess measurement correlations on different X-ray views on patients who have undergone or will undergo hip reconstruction surgery.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ENROLLING_BY_INVITATION
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
- Ability to provide informed consent.
- 40 patients: 20 preoperative THA, 20 postoperative THA;
- Sex: 20 men, 20 women;
- Age: 20 patients ≥ 70 years, 10 patients 50-70 years, 10 patients 18-50 years.
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Exclusion Criteria
- Patients with lumbosacral hardware, contralateral THA.
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Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Post-THA EOS X-Ray Subjects will be receiving EOS imaging after Total Hip Arthroplasty Pre-THA EOS X-Ray Subjects will be receiving EOS imaging prior to Total Hip Arthoplasty
- Primary Outcome Measures
Name Time Method Change in pelvic tilt (PT) Baseline, 8 hours, 4 weeks Measured from EOS imaging and AP x-ray, reported in degrees
Change in sacral slope (SS) Baseline, 8 hours, 4 weeks Measured from EOS imaging and AP x-ray, reported in degrees
Change in pelvic incidence (PI) Baseline, 8 hours, 4 weeks Measured from EOS imaging and AP x-ray, reported in degrees
Change in symphysis to sacrococcygeal junction distance (PSCD) Baseline, 8 hours, 4 weeks Measured from EOS imaging and AP x-ray, reported in millimeters (mm)
Change in lumbar lordosis (LL) Baseline, 8 hours, 4 weeks Measured from EOS imaging and AP x-ray, reported in degrees
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Mayo Clinic Rochester
🇺🇸Rochester, Minnesota, United States