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Completed
NCT04903860
Comparison of the Use of Conventional Ancillary Reaming and Single-use Ancillary Reaming Material in Total Hip Replacement
Conditions: Total Hip Replacement, Coxarthrosis
Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Phase: NA
Enrollment: 40
Sponsor: University Hospital, Clermont-Ferrand
Location: CHU clermont-ferrand Clermont-Ferrand
Summary
The main objective of the study is to compare the use of single-use ancillary reaming material during total hip replacement and conventional reusable ancillary reaming material.
The assessment will focus on the medico-economic differences found in this prospective randomized study
Eligibility Criteria
Inclusion Criteria:
* \- Patient, male or female, over 18 years of age, eligible for a first-line total hip replacement for isolated coxarthrosis
* Patient registered to the national health system
* Patient able to understand information about the protocol and answer to questionnaire
Exclusion Criteria:
* Pregnant, breastfeeding or potentially pregnant woman
* Major disability
* History of hip replacement surgery
* Any surgical and/or anesthetic contraindication, or any condition deemed by the investigator to be incompatible with the research.
* Morbid obesity as defined by body mass index (BMI) \>40 kg.m-2
* History of recent infection at the surgical site
* Surgical contraindication
* Refusal to participate
Source: ClinicalTrials.gov (NCT04903860). StuddyBuddy aggregates publicly available trial information.