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

• Status: Completed
• Trial end date: 2007-06-01
• Target enrollment: 0
• Participant gender: All

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 overnight stays.

• Phase: Phase 2/Phase 3
• Accepts Healthy Volunteers?: Accepts Healthy Volunteers

Details

• Lead Sponsor: Mayo Clinic
• Collaborator: Axcan Pharma

Criteria

1. Non-pregnant, non-breastfeeding females;

2. 18- 45 years old

3. Body mass index between 20 and 32 kg/m2

4. No alarm indicators on clinical assessment (weight loss of more than 7kg, bleeding, recent recurrent vomiting, progressive dysphagia).

5. No history suggestive of small bowel obstruction