drugset / Trial / NCT01657578

Optimal Dosing of Omeprazole in Neonates

NCT01657578

Phase 2 Completed 55 enrolled Assistance Publique - Hôpitaux de Paris
Non-randomizedSingle-groupQuadruple-blindTreatment

Summary

"The principal aim of this trial is to determine the minimum effective dose of omeprazole in neonates with GERD objectively diagnosed by a 24-h intra-oesophageal pH monitoring (pHmetry), to obtain a short-term efficacy in the pHmetry of control performed 72 hrs ± 24 after initiation of omeprazole. The secondary objectives of the study were: (1) to assess the efficacy of omeprazole upon other pHmetry parameters, (2) to characterize the population pharmacokinetics and pharmacogenetics of omeprazole, (3) to evaluate the effect of omeprazole upon oro-pharyngeal pH monitoring and (4) to assess the short-term safety of use of omeprazole in neonates."

Timeline

Start
2007-06
Primary completion
2010-12
Completion
2012-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Omeprazole Other / unclassified 1 mg/kg
Subject Omeprazole Other / unclassified 1.5 mg/kg
Subject Omeprazole Other / unclassified 2 mg/kg
Subject Omeprazole Other / unclassified 2.5 mg/kg
Subject Omeprazole Other / unclassified 3 mg/kg