About this trial
The goal of this clinical trial is to compare the gastro-intestinal biopotentials recorded with a homemade device using surface electrodes placed on the abdomen in healthy volunteers, Crohn's disease patients without fibrosis, Crohn's disease patients with fibrosis and in functional gastrointestinal disorders (FGID) patients.
The main question it aims to answer is:
• Is there any differences in the gastro-intestinal biopotentials between the different populations under study?
It aims to answer two secondary questions:
* Are the gastro-intestinal biopotentials comparable to the Harvey-Bradshaw Index, MRI and biological data for patients with Crohn's disease? * Are the gastro-intestinal biopotentials comparable to Rome IV criteria for functional gastrointestinal disorders patients?
Participants will undertake two recordings made with the device. The first one will last 1 hour and 30 minutes and will occurs while the participants are fasting. Then, the participants will eat a standardized meal. Finally, the second recording will take place after the meal ingestion and will last 1 hour and 30 minutes while the participants are in postprandial state.
Eligibility criteria
Qualifiers
Person age > 18 years
Person has been fasting for at least 12 hours
Person who has received full information on the organization of the research and has not objected to the use of this data.
Person affiliated to or beneficiary of a social security plan
Disqualifiers
Person having a pacemaker
Person suffering from a sensory disorder making insensitive to pain on the skin
Person suffering from a mental or motor disorders creating uncontroled movements
Person being allergic to one or more component of the device
Trial design
Treatments tested in this trial
- Gastro-intestinal biopotentials recording