Skip to content

Reliability of IUS in Crohn's Disease

Reliability of IUS in Crohn's Disease

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06833450
Acronym
LOTUS
Enrollment
30
Registered
2025-02-18
Start date
2022-01-19
Completion date
2026-02-28
Last updated
2025-02-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Crohn Disease (CD)

Keywords

Crohn's disease, intestinal ultrasound, bowel wall thickness

Brief 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.

Interventions

Transabdominal intestinal ultrasound

Sponsors

Centre Hospitalier Universitaire, Amiens
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
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)

Design outcomes

Primary

MeasureTime frameDescription
Number of different IUS parameters between two operators1 yearTo assess in patients with CD the variability of IUS parameters between two operators

Countries

France

Contacts

Primary ContactMathurin Fumery, Pr
Fumery.mathurin@chu-amiens.fr33+3 22 08 88 40

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026