Actively Recruiting
Total Hip Arthroplasty: Fluoroscopy vs Freehand
Led by Ente Ospedaliero Cantonale, Bellinzona · Updated on 2025-08-08
84
Participants Needed
1
Research Sites
144 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The aim of the study is to compare total hip arthroplasty intervention executed with or without the use of intraoperative fluoroscopy in terms of positioning of the hip prosthesis. The comparison will be made on post-operative follow-up X-ray performed as per clinical practice, in order to verify if intraoperative fluoroscopy provides better prosthesis components positioning or not.
CONDITIONS
Official Title
Total Hip Arthroplasty: Fluoroscopy vs Freehand
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients undergoing unilateral primary THA through DAA
- Patients aged 18-90 years old
- Patients with a BMI >18 and <35
- Patients able to provide informed consent
- Informed consent documented by signature
You will not qualify if you...
- Revision THA
- Women who are pregnant or breastfeeding
- Presence of other clinically significant concomitant disease states (ASA IV)
- Previous enrolment into the current study
- Enrolment of the investigator, family members, employees, or dependents
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Ente Ospedaliero Cantonale
Lugano, Canton Ticino, Switzerland, 6900
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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