ConditionIntraoperative Fluoroscopy
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-90
SponsorEnte Ospedaliero Cantonale, Bellinzona
About this trial
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.
Eligibility criteria
Qualifiers
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.
Disqualifiers
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.
Trial design
Treatments tested in this trial
- Intraoperative fluoroscopy
Treatment groups
84 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov