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Clinical Trials in France / NCT04846712
Recruiting Observational

Interest of Ultrasound in the Diagnosis of Severity of Lateral Ankle Sprain

NCT04846712 · tracked via the Priya Life Science France tracker
Sponsor
Centre Hospitalier Universitaire de Saint Etienne
Phase
Observational
Started
2021-12-01
Last updated
2024-08-29

Condition(s) studied

Ankle Sprains

Investigational drug(s) / intervention(s)

Collect data of medical record

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.

Study 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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
60 Years
Healthy volunteers
No
Inclusion Criteria: * First ankle sprain with sport or work disability Exclusion Criteria: * Patient with fractures, dislocation or hyperlaxity * Previous ankle sprain

Primary outcome measure(s)

  • Severity score by ultrasound (US) assesment — Day: 14 after Ankle Sprain.
    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

Trial sites (1)

FacilityCityRegionStatus
CHU Saint-Etienne Saint-Etienne France Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04846712 on ClinicalTrials.gov ↗ ← All trials in France