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Recruiting Not applicable

Reliability of IUS in Crohn's Disease

NCT06833450 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2022-01-19
Last updated
2025-02-18

Condition(s) studied

Crohn Disease (CD)

Investigational drug(s) / intervention(s)

Transabdominal intestinal ultrasound

Transabdominal intestinal ultrasound: Transabdominal intestinal ultrasound

Study summary

Transabdominal intestinal ultrasound (IUS) is gaining acceptance as a point-of-care test to objectively assess disease activity in Crohn's disease (CD).

In order to incorporate individual parameters in a future definition of transmural healing, and for the consistent application of IUS as a modality to assess treatment outcomes and establish therapeutic targets to ensure comparability between future studies, the inter-observer agreement should be determined for all relevant parameters.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Crohn's disease evolving for at least 1 months * Patient older than 18 years * Patient covered by French national health insurance * Written informed consent Exclusion Criteria: * Pregnant women or breastfeeding * Minor * Patient deprived of liberty by administrative or judicial decision or placed under judicial protection (guardianship or supervision)

Primary outcome measure(s)

  • Number of different IUS parameters between two operators — 1 year
    To assess in patients with CD the variability of IUS parameters between two operators

Trial sites (1)

FacilityCityRegionStatus
CHU d'Amiens Amiens France Recruiting
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 NCT06833450 on ClinicalTrials.gov ↗ ← All trials in France