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NCT05361928 Clinical Trial

IS ElastomEtry Useful in Muscle Lesion evaluaTion-REPROducibility Study

Muscle Injury Clinical Trial

— ISEULT-Repro  

Official title:
IS ElastomEtry Useful in Muscle Lesion evaluaTion-REPROducibility Study

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05361928
Other study ID # ISEULT (29BRC20.0211)
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 10, 2021
Est. completion date June 9, 2021

Study information
Verified date May 2022
Source University Hospital, Brest
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Our objective is to evaluate the inter and intra observer reproducibility of the measure of elasticity using Acoustic Radiation Force Impulse (ARFI) ultrasonography of mucles of patients with and without hamstring injury. 76 patients will be evaluated cross sectionally twice by two ultrasonographists.

Description:

Muscle trauma mainly results from sporting activities and accounts for 10 to 55% of sports injuries. Information on ARFI muscle trauma management is scarce. The present study sought to assess the initial ARFI characteristics of muscle in sports people with and without injury. Our objective here is to evaluate the inter and intra observer reproducibility of the measure of elasticity using Acoustic Radiation Force Impulse (ARFI) ultrasonography of muscles of patients with and without hamstring injury. 76 patients will be evaluated cross sectionally twice by two ultrasonographists(and then we will evaluate the evolution after 3 months for patient with injury according to the ARFI results).

Recruitment information / eligibility
Status Completed
Enrollment 31
Est. completion date June 9, 2021
Est. primary completion date June 9, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: - Patients justifying an ultrasound evaluation for suspicion of muscle injury Exclusion Criteria: - Inflammatory muscle disease

Study Design

Related Conditions & MeSH terms

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 Elasticity ultrasound Inclusion
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