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Variability in Spinopelvic Parameters Among Patients Undergoing Total Hip Arthroplasty

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Mayo Clinic

Status

Completed

Conditions

Osteoarthritis, Hip

Treatments

Diagnostic Test: EOS X-Ray

Study type

Interventional

Funder types

Other

Identifiers

NCT05212090
21-011655

Details and patient eligibility

About

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.

Enrollment

40 patients

Sex

All

Ages

18 to 99 years old

Volunteers

No Healthy Volunteers

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.

Trial design

Primary purpose

Health Services Research

Allocation

Non-Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

40 participants in 2 patient groups

Pre-THA
Other group
Description:
Subjects will be receiving EOS imaging prior to Total Hip Arthroplasty (THA)
Treatment:
Diagnostic Test: EOS X-Ray
Post-THA
Other group
Description:
Subjects will be receiving EOS imaging after Total Hip Arthroplasty (THA)
Treatment:
Diagnostic Test: EOS X-Ray

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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