Digestive System Disorders Clinical Trial
Official title:
An Open-label, Single Centre, Randomised, Cross-over Study to Examine the Effect of Ulimorelin on the Pharmacokinetics of Midazolam After Repeat Dose Administration of Ulimorelin in Healthy Volunteers
An open-label, single centre, randomised, cross-over study to examine the effect of ulimorelin on the pharmacokinetics of midazolam after repeat dose administration of ulimorelin in healthy volunteers.
Ulimorelin is a first-in-class new chemical entity. It is a ghrelin agonist with
gastroprokinetic activity being developed as an intravenous therapy to be used in the
treatment of gastrointestinal (GI) hypomotility disorders such as post-operative ileus (POI)
and gastroparesis.
POI is a transient disruption of co-ordinated bowel motility that contributes to patient
morbidity, discomfort and prolonged recovery times. POI most commonly occurs after abdominal
surgery and annually, POI is the main determinant of length of hospital stay after major
abdominal surgery and a factor in patient hospital re-admissions, increased healthcare
resource use and cost, and decreased patient satisfaction. Current strategies to attenuate
POI are aimed at enhanced recovery after surgery (ERAS) or "fast track". These are
multimodal care protocols designed to reduce the impact of external and internal factors on
POI duration. Recently, fewer complications and a quicker return to work and normal
activities for patients who have had ERAS programmes implemented have been reported. In
spite of these strategies only up to 20% of subjects undergoing partial bowel resection
recover GI function within 72 hours after surgery.
;
Allocation: Randomized, Endpoint Classification: Pharmacokinetics Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Diagnostic
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT01770808 -
A Study to Determine if Aquamin (as AquaCal and AquaPT) Improves Digestive Discomfort
|
N/A | |
Completed |
NCT01405599 -
Evaluation of the Pharmacokinetics of Ulimorelin in Subjects With Hepatic Impairment and Healthy Subjects
|
Phase 1 | |
Unknown status |
NCT01318928 -
The Treatment of Periodontal Diseases
|
Phase 4 | |
Completed |
NCT01304394 -
Safety During Use of Paediatric Triple Chamber Bag Formulas
|
Phase 3 | |
Completed |
NCT01485328 -
Protocol: Phytomedicine-AMARGOL®, Clinical Trial for Efficacy Proof on Therapeutics
|
Phase 3 |