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NCT05212090 Clinical Trial

Variability in Spinopelvic Parameters Among Patients Undergoing Total Hip Arthroplasty

Osteoarthritis, Hip Clinical Trial

Official title:
Study-Dependent Variability in Spinopelvic Parameters Among Patients Undergoing Total Hip Arthroplasty

Clinical Trial Details — Status: Enrolling by invitation

Administrative data
NCT number NCT05212090
Other study ID # 21-011655
Secondary ID
Status Enrolling by invitation
Phase N/A
First received
Last updated
Start date February 1, 2022
Est. completion date February 2025

Study information
Verified date January 2024
Source Mayo Clinic
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.

Recruitment information / eligibility
Status Enrolling by invitation
Enrollment 40
Est. completion date February 2025
Est. primary completion date February 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years to 99 Years
Eligibility 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. Exclusion Criteria: - Patients with lumbosacral hardware, contralateral THA.

Study Design

Related Conditions & MeSH terms

Intervention

Diagnostic Test:
• EOS X-Ray
Repeated AP Pelvis x-ray and Lateral Lumbar EOS x-ray

Locations
Country Name City State
United States Mayo Clinic Rochester Rochester Minnesota

Sponsors (1)
Lead Sponsor Collaborator
Mayo Clinic

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Change in pelvic incidence (PI) Measured from EOS imaging and AP x-ray, reported in degrees Baseline, 8 hours, 4 weeks
Primary Change in symphysis to sacrococcygeal junction distance (PSCD) Measured from EOS imaging and AP x-ray, reported in millimeters (mm) Baseline, 8 hours, 4 weeks
Primary Change in pelvic tilt (PT) Measured from EOS imaging and AP x-ray, reported in degrees Baseline, 8 hours, 4 weeks
Primary Change in sacral slope (SS) Measured from EOS imaging and AP x-ray, reported in degrees Baseline, 8 hours, 4 weeks
Primary Change in lumbar lordosis (LL) Measured from EOS imaging and AP x-ray, reported in degrees Baseline, 8 hours, 4 weeks
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