The Effect of Prucalopride (Resolor®) on Gastric Motor Function and Gastric Sensitivity
Gastrointestinal Motility Disorder, Dyspepsia
About this trial
This is an interventional treatment trial for Gastrointestinal Motility Disorder focused on measuring gastric accommodation, gastric sensitivity, gastric compliance, nutrient tolerance
Eligibility Criteria
Inclusion Criteria:
- Healthy volunteers, male and females, between 18-60 years old
Exclusion Criteria:
Subjects that:
- They are older than 60 years old.
- Have severely decreased kidney function.
- Have severely decreased liver function.
- Have severe heart disease, for example a history of irregular heartbeats, angina or heart attack.
- Have severe lung disease.
- Have severe psychiatric illness or neurological illness.
- Have any gastrointestinal disease
- Women that are pregnant or breastfeeding.
- Have a rare hereditary problems of galactose intolerance, the Lapp lactase deficiency or glucose-galactose malabsorption (Resolor tablets contain lactose).
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Placebo Comparator
Experimental
Placebo
Prucalopride
Placebo is an opaque empty gel capsule obtained from the UZ Gasthuisberg pharmacy. These capsules are composed of 100% gelatine that will rapidly dissolve (disintegration time is 15 minutes) in the stomach without affecting the gastric motor function.
2 mg, Resolor®, Shire, Belgium Prucalopride (2 mg) is rapidly absorbed; after a single oral dose of 2 mg Cmax was attained in 2-3 hours. The absolute oral bioavailability is >90%. Concomitant intake of food does not influence the oral bioavailability of prucalopride.