Phenylephrine Dose and Mode of Administration for Spinal Anesthesia Induced Hypotension

Withdrawn before enrolling · Not applicable

Conditions studied: Complications; Cesarean Section, Spinal Anesthetics Causing Adverse Effects in Therapeutic Use

In brief

Three different regimens of phenylephrine are being evaluated to see if one is superior over the other in the maintenance of cardiac output while keeping normotension and/or treating hypotension experienced when receiving spinal anesthesia for cesarean delivery.

Key facts

Study ID

NCT02101047

Run by

Wake Forest University Health Sciences

People needed

0

Starts

2015-08-01

Expected to finish

2016-12-31

Last updated by the study team

2017-11-08

Who can join

Age: 18 and older, up to 45. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• scheduled for cesarean delivery age >/=18 years of age >/= 37 weeks EGA ASA status I-III

You may not qualify if…

• allergy to medications used in the study non-English speaking

Where it is running

• Novant Health Forsyth Medical Center — Winston-Salem, North Carolina, United States

Full record on ClinicalTrials.gov

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