Variability in Spinopelvic Parameters Among Patients Undergoing Total Hip Arthroplasty

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-02-01

Study Completion Date

2025-03-12

Brief Summary

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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.

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Detailed Description

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Conditions

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Osteoarthritis, Hip

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

NONE

Study Groups

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Pre-THA

Subjects will be receiving EOS imaging prior to Total Hip Arthroplasty (THA)

Group Type OTHER

EOS X-Ray

Intervention Type DIAGNOSTIC_TEST

Repeated Anteroposterior (AP) Pelvis x-ray and Lateral Lumbar EOS x-ray

Post-THA

Subjects will be receiving EOS imaging after Total Hip Arthroplasty (THA)

Group Type OTHER

EOS X-Ray

Intervention Type DIAGNOSTIC_TEST

Repeated Anteroposterior (AP) Pelvis x-ray and Lateral Lumbar EOS x-ray

Interventions

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EOS X-Ray

Repeated Anteroposterior (AP) Pelvis x-ray and Lateral Lumbar EOS x-ray

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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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.