Status:

COMPLETED

The Effects of Dietary Intervention on Gastrointestinal Function in Patients With Anorexia Nervosa and Obesity

Lead Sponsor:

University of Zurich

Collaborating Sponsors:

Schweizerischer Nationalfonds

Conditions:

Anorexia Nervosa

Obesity

Eligibility:

All Genders

18-40 years

Phase:

NA

Brief Summary

Diseases characterized by abnormal low and high body weight are common in the community and are associated with significant morbidity, mortality and health care related costs. Genetic, dietary, socia...

Eligibility Criteria

Inclusion

  • In addition to satisfying specific DSMIV criteria for anorexia nervosa (B1, B2) or WHO criteria for obesity (C1), or obesity and diabetes mellitus type II (C2), general inclusion criteria include:
  • aged at least 18 and not more than 40 years
  • able to communicate well with the investigators and provide written consent
  • no physical co-morbidity requiring active treatment, in particular diabetes mellitus, impairment of liver or kidney function (subjects with diabetes mellitus type II are eligible for study group C2)
  • no psychiatric (DSM IV) disorders limiting the ability to comply with study requirements
  • no use of medications influencing upper GI motility within one week of the study (i.e. nitrates, prokinetic drugs, macrolide antibiotics). Acid suppression and antihypertensive medication beta-blocker, calcium channel blockers are acceptable.
  • no evidence of current drug or alcohol abuse
  • no history of gastrointestinal disease or surgery except appendicectomy or hernia repair
  • females will take a urine pregnancy test before each study, any participant with a positive pregnancy test will be excluded (females will be investigated always in the same menstrual phase)
  • Exclusion criteria:
  • • pregnancy

Exclusion

    Key Trial Info

    Start Date :

    September 1 2010

    Trial Type :

    INTERVENTIONAL

    Allocation :

    ACTUAL

    End Date :

    November 1 2012

    Estimated Enrollment :

    60 Patients enrolled

    Trial Details

    Trial ID

    NCT00946816

    Start Date

    September 1 2010

    End Date

    November 1 2012

    Last Update

    November 14 2012

    Active Locations (1)

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    University Hospital Zurich, Gastroenterology and Hepatology

    Zurich, Canton of Zurich, Switzerland, 8091