WithdrawnNot Applicable

Phenylephrine Dose and Mode of Administration for Spinal Anesthesia Induced Hypotension

Stopped: lack of eligible participant

United States0Started 2015-08

Plain-language summary

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.

Who can participate

Age range18 Years – 45 Years

SexFEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * scheduled for cesarean delivery age \>/=18 years of age \>/= 37 weeks EGA ASA status I-III Exclusion Criteria: * allergy to medications used in the study non-English speaking

What they're measuring

Magnitude of cardiac output changes

Timeframe: 0-90 minutes

Trial details

NCT IDNCT02101047

SponsorWake Forest University Health Sciences

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2016-12-31

View on ClinicalTrials.gov More Complications; Cesarean Section trials