drugset / Trial / NCT02510976

Prucalopride Versus Placebo in Gastroparesis

NCT02510976 ↗

Phase 4 Terminated 60 enrolled Universitaire Ziekenhuizen KU Leuven
RandomizedCrossoverQuadruple-blindTreatment

Summary

Controlled cross-over study of prucalopride 2 mg daily or placebo in gastroparesis (idiopathic or diabetic). Patients will be randomized to 4 week treatment with the first regimen (double-blind), followed by a 2-week washout and 4 week treatment with the second regimen in cross-over.

Timeline

Start
2011-11
Primary completion
2021-01-08
Completion
2021-01-08

Outcome

Outcome not reported

Stopped (Enrollment): “Prematurely stopped due to slow recruitment and expiry of study drug.”

Drugs

EvaluationDrugModalityDoseRoute
Comparator Prucalopride Small molecule 2 mg —

Indications