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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04846712
Other study ID # IRBN1382021/CHUSTE
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date December 1, 2021
Est. completion date September 2027

Study information

Verified date July 2023
Source Centre Hospitalier Universitaire de Saint Etienne
Contact Thomas NERI, MD
Phone (0)477127849
Email thomas.neri@chu-st-etienne.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Ankle sprain is a frequent and widely trivialized trauma. Misdiagnosed or poorly treated, it can recur and thus develop into chronic ankle instability. It can be associated with complications which, if not detected early, can lead to long-term sequelae.


Description:

The hypothesis of this study is that ultrasound can better characterize the severity stages of the sprain and can diagnose complications that may have gone unnoticed on physical examination. Patients were assessed clinically: demographics, history, clinical examination, functional scores. An ultrasound and an MRI were done during the first month to check for complications. The main objective is to assess the value of ultrasound in the diagnosis of the severity of the lateral ankle sprain. The secondary objective is to compare an ultrasound assessment of severity with a clinical assessment and Magnetic Resonance Imaging (MRI).


Recruitment information / eligibility

Status Recruiting
Enrollment 50
Est. completion date September 2027
Est. primary completion date September 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: - First ankle sprain with sport or work disability Exclusion Criteria: - Patient with fractures, dislocation or hyperlaxity - Previous ankle sprain

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Collect data of medical record
Collect data of medical record: initial physical examination, ultrasound (US), Magnetic Resonance Imaging (MRI), physical examination at 30 days, physical examination at 3 months, physical examination at 6 months and final examination at 12 months.

Locations

Country Name City State
France CHU Saint-Etienne Saint-Étienne

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire de Saint Etienne

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Severity score by ultrasound (US) assesment Collected in medical record.
This system utilises a classification that is based on injury severity related to the amount of tissue damage and associated functional loss. It categorises muscle injuries into three grades, ranging from grade 1 with no appreciable tissue tear, grade 2 with tissue damage and reduced strength of the musculotendinous unit and grade 3 with complete tear of musculotendinous unit and complete loss of function
Day: 14 after Ankle Sprain.
Secondary Severity score by Magnetic Resonance Imaging (MRI) assesment Collected in medical record.
This system utilises a classification that is based on injury severity related to the amount of tissue damage and associated functional loss. It categorises muscle injuries into three grades, ranging from grade 1 with no appreciable tissue tear, grade 2 with tissue damage and reduced strength of the musculotendinous unit and grade 3 with complete tear of musculotendinous unit and complete loss of function
Day: 14 after Ankle Sprain.
Secondary Severity score by radiologist assesment Collected in medical record.
Empirical score : low, mild, severe
Day: 30, 90, 180, 365 after Ankle Sprain.
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