drugset / Trial / NCT01236482

Oxytocin in Cesarean Delivery

NCT01236482

Phase 4 Unknown 80 enrolled Hadassah Medical Organization
RandomizedParallel-groupQuadruple-blindTreatment

Summary

In this study the investigators hypothesize that infused combinations of oxytocin and ergometrine will exhibit fewer cardiac and neurological side effects than equipotent infusion of oxytocin alone. In order to perform this study the investigators perform the following steps: 1. The investigators validate a quantitative measure of uterine tone as our primary endpoint. 2. The investigators use this endpoint measure in order to determine equipotential doses of different tocotonic drug regimens, based on the ED50 for each. 3. Using equipontial ratios based on the ED50, the investigators compare hemodynamic and other side effects of these tocotonic drug regimes. Plasma levels of oxytocin will be measured.

Timeline

Start
2010-11
Primary completion
2011-05
Completion
2011-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Oxytocin Peptide 0.1 iu/kg
Subject ergometrine Unknown 2 ug/kg

Indications

No indication recorded.