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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

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View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT04903860). StuddyBuddy aggregates publicly available trial information.