drugset / Trial / NCT01481740

Preventing Hypotension in Parturients With an Elevated Body Mass Index (BMI)

NCT01481740

Phase 4 Completed 178 enrolled IWK Health Centre Duke University · collab
RandomizedSingle-groupQuadruple-blindTreatment

Summary

Previous research regarding the use of phenylephrine has excluded obese subjects (BMI \>35). This subgroup of patients represents a large portion of the obstetric patient population locally and nationally. It is unclear whether previous research should be extrapolated to the obese patient population. This study is being done to compare the incidence of hypotension, intraoperative nausea and vomiting, and neonatal acidosis between obese patients who receive a prophylactic phenylephrine infusion versus those who receive phenylephrine boluses for the treatment of established hypotension. This study will help us determine whether using a phenylephrine infusion or a phenylephrine bolus is the best way to prevent/treat spinal induced hypotension during cesarean deliveries in obese patients.

Timeline

Start
2010-11
Primary completion
2014-12
Completion
2014-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Phenylephrine Small molecule 50 ug
Subject Phenylephrine Small molecule 100 ug

Indications