MedTrace Logo

Comparison of the Use of Conventional Ancillary Reaming and Single-use Ancillary Reaming Material in Total Hip Replacement

NCT04903860 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2022-07-28

No results posted yet for this study

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

Conditions

  • Total Hip Replacement
  • Coxarthrosis

Interventions

DEVICE

total hip replacement with single use ancillary

Comparison of the use of conventional ancillary reaming and single-use ancillary reaming material in total hip replacement

DEVICE

total hip replacement with conventional ancillary

Comparison of the use of conventional ancillary reaming and single-use ancillary reaming material in total hip replacement

Sponsors & Collaborators

  • Groupe Lépine

    collaborator UNKNOWN

  • University Hospital, Clermont-Ferrand

    lead OTHER

Principal Investigators

  • Roger ERIVAN · University Hospital, Clermont-Ferrand

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-07-12
Primary Completion
2022-07-27
Completion
2022-07-27

Countries

  • France

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04903860 on ClinicalTrials.gov