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Can live X-Ray guidance make hip implants fit better?
NCT ID NCT05653687
First seen Sep 11, 2026 · Last updated Sep 11, 2026
Summary
Researchers are testing whether using intraoperative fluoroscopy, a live X-ray video, helps surgeons position hip replacement components more accurately than the standard freehand method. The trial enrolls 84 adults undergoing a first total hip replacement through a direct anterior approach. After surgery, the team measures implant angles on routine follow-up X-rays to compare the two techniques.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- intraoperative fluoroscopy, a real-time X-ray video used during surgery
- What this could lead to
- If fluoroscopy helps, surgeons could place hip implants more accurately, which may reduce the chance of dislocation or uneven wear and could lead to fewer repeat operations.
- What could go wrong
- This is a small, single-center study of 84 people, so the results may not apply to all surgeons or hospitals. Fluoroscopy adds X-ray exposure and operating time, and any accuracy benefit might be too small to change how most hip replacements are done.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 84 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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May 2023
- Expected to finish
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Mar 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 90 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * 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 as documented by signature. Exclusion Criteria: * Revision THA. * Women who are pregnant or breast feeding. * Presence of other clinically significant concomitant disease states (ASA IV). * Previous enrolment into the current study. * Enrolment of the investigator, his/her family members, employees and other dependent persons.
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Ente Ospedaliero Cantonale
RECRUITINGLugano, Canton Ticino, 6900, Switzerland