Status:

COMPLETED

A Study to Evaluate the Effect of a Medicine on Gastric Functions in Healthy Volunteers.

Lead Sponsor:

Mayo Clinic

Collaborating Sponsors:

Axcan Pharma

Conditions:

Healthy Volunteers

Eligibility:

All Genders

18-45 years

Phase:

PHASE2

PHASE3

Brief Summary

A 7 day study which involves 2 nutrient drink tests, an ECG, a Scintigraphy scan, and a Sect scan. This study requires the participant to make 4 visits to the GCRC in the Charlton building but no over...

Detailed Description

A screening interview and symptoms assessment by the Bowel Disease Questionnaire (BDQ) and consent will be obtained prior to the studies at the testing facility (General Clinical Research Center, 7th ...

Eligibility Criteria

Inclusion

  • Non-pregnant, non-breastfeeding females;
  • 18- 45 years old
  • Body mass index between 20 and 32 kg/m2
  • No alarm indicators on clinical assessment (weight loss of more than 7kg, bleeding, recent recurrent vomiting, progressive dysphagia).
  • No history suggestive of small bowel obstruction

Exclusion

    Key Trial Info

    Start Date :

    November 1 2005

    Trial Type :

    INTERVENTIONAL

    Allocation :

    ACTUAL

    End Date :

    June 1 2007

    Estimated Enrollment :

    45 Patients enrolled

    Trial Details

    Trial ID

    NCT00308399

    Start Date

    November 1 2005

    End Date

    June 1 2007

    Last Update

    March 23 2011

    Active Locations (1)

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    Mayo Clinic

    Rochester, Minnesota, United States, 55905

    A Study to Evaluate the Effect of a Medicine on Gastric Functions in Healthy Volunteers. | DecenTrialz