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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01095042
Other study ID # 0817
Secondary ID 2008-A00994-51
Status Completed
Phase N/A
First received February 22, 2010
Last updated January 27, 2014
Start date October 2008
Est. completion date May 2013

Study information

Verified date January 2014
Source University Hospital, Grenoble
Contact n/a
Is FDA regulated No
Health authority France: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis)
Study type Interventional

Clinical Trial Summary

The study aims at showing that the susceptibility in the stress is more raised at the person affected digestive pathologies (SII or IBD) in forgiveness than healthy subjects.


Description:

The objective of the study which we wish to lead consists in looking for, at the patients SII and IBD in forgiveness, the existence of a correlation between the rate of cortisol(Hormone of the stress) and the level of HRV (Heart Rate Variability) to estimate the inhibitive fronto-amygdalien tonus.

So we make the hypothesis that the persons affected by digestive pathologies of type SII or IBD would present an emotional and physiological vulnerability more important than unhurt subjects of pathologies.


Recruitment information / eligibility

Status Completed
Enrollment 120
Est. completion date May 2013
Est. primary completion date May 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 20 Years to 60 Years
Eligibility Inclusion Criteria:

- Patients with SII :Membership to the Social Security,SII defined according to the criteria Rome III.

- Patients with IBD :Membership to the Social Security,patients with a ulcerative colitis(UC) or a Crohn's disease (CD)ileal and/or colic.

Exclusion Criteria:

- Existence of a severe affectation on the general plan (cardiac,respiratory,hematological,renal,hepatic,cancerous),

- Subject diabetic,

- Pregnant or breast-feeding woman,

- Subject included in another clinical and\or therapeutic trial or having been included in a clinical and\or therapeutic trial for less than a month,

- Subject presenting a psychiatric pathology evident,

- Person under guardianship.

Study Design

Allocation: Non-Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Supportive Care


Intervention

Behavioral:
emotion
Show that the susceptibility in the stress (recording of Heart Rate Variability;viewing films;...) is more important at the person affected by digestive pathologies (SII or IBD) in forgiveness than to unhurt subjects of pathologies.

Locations

Country Name City State
France Hôpital Michallon-CHU Grenoble Grenoble

Sponsors (3)

Lead Sponsor Collaborator
University Hospital, Grenoble Association François Aupetit, French society of Gastroenterology

Country where clinical trial is conducted

France, 

References & Publications (3)

Graff LA, Walker JR, Clara I, Lix L, Miller N, Rogala L, Rawsthorne P, Bernstein CN. Stress coping, distress, and health perceptions in inflammatory bowel disease and community controls. Am J Gastroenterol. 2009 Dec;104(12):2959-69. doi: 10.1038/ajg.2009.529. Epub 2009 Sep 15. — View Citation

Pellissier S, Dantzer C, Canini F, Mathieu N, Bonaz B. Psychological adjustment and autonomic disturbances in inflammatory bowel diseases and irritable bowel syndrome. Psychoneuroendocrinology. 2010 Jun;35(5):653-62. doi: 10.1016/j.psyneuen.2009.10.004. Epub 2009 Nov 11. — View Citation

Pellissier S, Dantzer C, Canini F, Mathieu N, Bonaz B. Toward a definition of a global psycho-physiological criterion of vulnerability to relapse in inflammatory bowel diseases. Am J Gastroenterol. 2010 Jun;105(6):1446-7. doi: 10.1038/ajg.2009.763. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary RATE PLASMATIQUE OF CORTISOL COUPLED WITH THE CARDIAC VARIABILITY 24 MONTHS No
Secondary SCORES OF DEPRESSIVE SYMPTOMATOLOGIE AND ANXIETY, RATE PLASMATIQUES OF CATECHOLAMINES, LEPTINE, ADIPONECTINE AND PRO-INFLAMMATORY CYTOKINES. 24 MONTHS No
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