Total Hip Arthroplasty: Fluoroscopy vs Freehand

Last updated: July 16, 2024
Sponsor: Ente Ospedaliero Cantonale, Bellinzona
Overall Status: Active - Recruiting

Phase

N/A

Condition

N/A

Treatment

Intraoperative fluoroscopy

Clinical Study ID

NCT05653687
ORL-ORT-036
  • Ages 18-90
  • All Genders

Study Summary

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

Inclusion

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

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 dependentpersons.

Study Design

Total Participants: 84
Treatment Group(s): 1
Primary Treatment: Intraoperative fluoroscopy
Phase:
Study Start date:
May 22, 2023
Estimated Completion Date:
March 31, 2026

Connect with a study center

  • Ente Ospedaliero Cantonale

    Lugano, Ticino 6900
    Switzerland

    Active - Recruiting

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