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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04587440
Other study ID # 29BRC20.0120
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date February 2, 2021
Est. completion date August 2, 2023

Study information

Verified date January 2022
Source University Hospital, Brest
Contact Eric Stindel, PUPH
Phone +33298347275
Email eric.stindel@chu-brest.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Total hip replacement is one of the most common surgical procedure in France. In 2010, an estimated 147 513 total hip procedures were performed. This number is constantly increasing. Although it is common, it can lead to many complications. The intra-prosthetic luxation is the second one after aseptic loosening. The luxation risk is multifactorial and depends on the relative orientation of femoral et acetabular components. This orientation is influenced by statics and dynamics parameters. So far, the literature shows that only static parameters are considered by surgeons. Thus, in reference to Lewinneck publication, which states that the luxation risk is lower if the cup is oriented with 15° +/- 10° of anteversion and 40°+/- 10° of inclination with respect to the anterior pelvic plan (APP). Defined by the two anterosuperior iliacs spines and pubic symphysis. However, this approach is only static and do not take into account the variations of pelvic plan orientation during everyday life. To consider these variations of pelvic inclination, it is possible to measure the angle between APP and the horizontal (in lying position) or the vertical (in standing position) plan. Several devices allow the measure of pelvic inclination but they all have important limits (EOS radiography, scanner or navigation). A new device has been developed in Brest to measure this inclination in several positions of the daily life.This software has already been tested in healthy volunteers and results demonstrate an excellent accuracy and reproducibility. The goal of this study is to described the dynamic of the pelvic bone thanks to this ultrasound based device, and to assess the amount of variation induced by hip replacement procedures.


Recruitment information / eligibility

Status Recruiting
Enrollment 53
Est. completion date August 2, 2023
Est. primary completion date February 2, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion criteria : - Patient with primary or secondary hip arthritis, at stage II to III of the radiological classification of Tönnis and for whom total hip replacement is indicated by surgeon. - Signed consent - Patient beneficiary of a social security plan Exclusion Criteria: - Patient Under 18 - Patient Under protective measure (guardianship, curatorship) or unable to consent - Patient requiring revision THR - Patient with geographic mobility plan before the end of the follow-up - Symptomatic contralateral hip - Symptomatic dorsolumbar rachis - Pelvis or spine surgery planed during the follow-up - Pregnant or nursing woman

Study Design


Intervention

Other:
Pelvic inclination measurement
Ultra-sound based measurements of the pelvic inclination lying, standing and seating position. EOX X-ray in seating position.

Locations

Country Name City State
France CHRU de Brest Brest

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Brest

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Variation of the pelvic incidence The main evaluation criterion is the variation of the pelvic incidence between pre- and post-operative total hip replacements Day 0 - Month 3
Secondary Analysis of the correlation between the variation in pelvic incidence while sitting, standing and lying down and the implant settings Assessed by EOS X-Ray. Day 0 - Month 3
Secondary Analysis of the correlation between variation in pelvic incidence while sitting, standing and lying down and clinical parameters (Harris hip score) Clinical examination (Harris hip score) will be performed at day 0 and month 3. Day 0 - Month 3
Secondary Analysis of the correlation between variation in pelvic incidence while sitting, standing and lying down and clinical parameters (EVA) Clinical examination (EVA) will be performed at day 0 and month 3. Day 0 - Month 3
Secondary Analysis of the correlation between variation in pelvic incidence while sitting, standing and lying down and clinical parameters (Hand-ground distance) Clinical examination (Hand-ground distance) will be performed at day 0 and month 3. Day 0 - Month 3
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