MedPath

Pelvic Inclination Measurement by Navigated Ultrasound

Not Applicable
Completed
Conditions
Arthroplasty, Replacement, Hip
Interventions
Other: Pelvic inclination measurement
Registration Number
NCT03555812
Lead Sponsor
University Hospital, Brest
Brief Summary

Prospective, multicenter, non-randomized study.

Primary endpoint : to confirm the proper functioning of the device in vivo by analyzing intra and interobserver reproducibility of repeated measurements on healthy controls.

Secondary endpoint : to describe the values of pelvic inclination while standing, sitting and lying in patients with severe hip osteoarthritis before and after total hip arthroplasty

After signing the inform consent form:

For the first endpoint (, 3 healthy volunteers of different morphotypes will have one consultation comprising :

* a medical examination

* 10 measurements of pelvic inclination in sitting position, 10 measurements of pelvic inclination in supine position and 10 measurements of pelvic inclination in standing position, each realized per three different operators. These measurements will be carried out with navigated ultrasound.

For the secondary endpoint, 30 patients awaiting for a hip replacement surgical intervention will realized one consultation the day before the intervention, and one consultation at 2 months after surgery, each comprising :

* a medical examination

* 3 measurements of pelvic inclination (1 standing, 1 sitting and 1 supine). These measurements will be carried out with navigated ultrasound.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
33
Inclusion Criteria

For primary endpoint

  • No medical or surgical history

  • Major healthy voluntary topic with

    • Body Mass Index (BMI) <20 for a subject
    • 24 <BMI <26 for a subject
    • BMI> 30 for a subject
  • Subject having signed an informed consent

For the secondary endpoint

  • Adult patient requiring total hip arthroplasty for severe hip osteoarthritis
  • Patient having signed an informed consent
Exclusion Criteria
  • Minor subject
  • Resumption of total hip prosthesis
  • Subject who can not express their consent to research
  • Presence of medical or surgical history for healthy volunteers

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Healthy volunteersPelvic inclination measurement* a medical examination * 10 measurements of pelvic tilt in sitting position, 10 measurements of pelvic tilt in supine position and 10 measurements of pelvic tilt in standing position, each performed by three different operators. These measurements will be done by ultrasound.
PatientsPelvic inclination measurementa consultation the day before surgery, and a consultation 2 months after surgery, each including: * a medical examination * 3 pelvic tilt measurements (1 standing, 1 sitting and 1 lying down). These measurements will be done by ultrasound.
Primary Outcome Measures
NameTimeMethod
Pelvic inclination measurementDay 0

The pelvic inclination measurement corresponds to the anterior pelvic plane also known as the Lewinnek's plane; defined by the plane between both anterior superior iliac spine and the pubic symphysis.

A Portable Ultrasound based Device is used for the Measurement of the Pelvic Tilt

Secondary Outcome Measures
NameTimeMethod
Variation of pelvic inclination before and after hip replacementMonth 2

The pelvic inclination measurement corresponds to the anterior pelvic plane also known as the Lewinnek's plane; defined by the plane between both anterior superior iliac spine and the pubic symphysis.

A Portable Ultrasound based Device is used for the Measurement of the Pelvic Tilt

Trial Locations

Locations (2)

Brest University Hospital

🇫🇷

Brest, France

Clinique de Keraudren

🇫🇷

Brest, France

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