drugset / Trial / NCT01657578
Optimal Dosing of Omeprazole in Neonates
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 | — |