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Olfactogustatory Perception, Eating Behaviour and Inflammation in Crohn's Disease (Smell&Crohn)

U

University Hospital Center (CHU) Dijon Bourgogne

Status

Completed

Conditions

Olfactogustatory Perception
Crohn's Disease

Treatments

Other: triangular test
Biological: blood sampling
Other: Questionnaires

Study type

Observational

Funder types

Other

Identifiers

NCT02859675
BRONDEL Ass INRA 2011

Details and patient eligibility

About

This study will improve our understanding of the mechanisms underlying anorexia in persons with Crohn's disease flare-ups. The practical spin-off from this research is potentially very important for the management of nutritional disorders associated with the disease by guiding diets towards foods that correspond to patients' preferences and/or to modified tastes. In addition, the results could lead to the identification of sensory markers that herald an inflammatory flare-up of the disease.

Enrollment

62 patients

Sex

Female

Ages

18 to 60 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

For patients :

Inclusion Criteria:

  • Age between 18 and 60 years,
  • Diagnosis of Crohn's disease according to clinical, endoscopic, histological, radiological and biochemical criteria as defined by the European Consensus Conference,
  • Men or women who have provided consent and willing to cooperate.

Exclusion Criteria:

  • Chronic inflammatory intestinal disease (CIID) other than Crohn's disease: haemorrhagic rectocolitis, undetermined colitis, microscopic colitis.
  • Intercurrent disease (diabetes and metabolic disease, liver cirrhosis, progressive cancer, acute or chronic infection, Human Immunodeficiency Virus HIV),
  • Organ failure (respiratory, heart, or renal failure, neurological disorders),
  • Intolerance to gluten,
  • Treatments (other than those used for Crohn's disease) able to interfere with food intake,
  • Aversion to foods consumed or smelled,
  • Poor understanding of cognitive tasks required.
  • Crohn's disease complicated by an abscess or infectious complication
  • Acute Crohn's disease defined by a CDAI score > 150

For Controls:

Inclusion Criteria:

  • Adult person
  • Without follow-up for a chronic pathology
  • Having given its consent

Exclusion Criteria:

  • Protected adult
  • Person not affiliated to a social security system
  • Pregnant or breastfeeding woman
  • Active smoker
  • No one who does not speak French
  • Taking treatment that interferes with taste or acts on the central nervous system

Trial design

62 participants in 3 patient groups

Crohn and anti-TNF treatment
Description:
Tests at 3 or 4 weeks after the beginning of anti-TNF treatment
Treatment:
Other: Questionnaires
Other: triangular test
Biological: blood sampling
Crohn and without anti-TNF treatment
Description:
tests performed according to patient availability
Treatment:
Other: Questionnaires
Other: triangular test
Biological: blood sampling
Control
Description:
tests performed according to patient availability
Treatment:
Other: Questionnaires
Other: triangular test
Biological: blood sampling

Trial contacts and locations

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Central trial contact

Laurent BRONDEL

Data sourced from clinicaltrials.gov

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