CompletedNot Applicable

Prevention of Hypotension During Cesarean Section

Greece82 participantsStarted 2019-02-16

Plain-language summary

The aim of this double-blind randomized study will be to compare a fixed-rate prophylactic noradrenaline infusion to a fixed-rate prophylactic phenylephrine infusion during elective cesarean section under combined spinal-epidural anesthesia

Who can participate

Age range18 Years – 48 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: * adult parturients, American Society of Anesthesiologists (ASA) I-II, singleton gestation\>37 weeks * elective cesarean section Exclusion Criteria: * Body Mass Index (BMI) \>40 kg/m2 * Body weight \<50 kg * Body weight\>100 kg * height\<150 cm * height\>180 cm * multiple gestation * fetal abnormality * fetal distress * active labor * cardiac disease * pregnancy-induced hypertension * thrombocytopenia * coagulation abnormalities * use of antihypertensive medication during pregnancy * communication or language barriers * lack of informed consent * contraindication for regional anesthesia

What they're measuring

incidence of bradycardia

Timeframe: intraoperative

Trial details

NCT IDNCT03842046

SponsorAretaieion University Hospital

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2019-08-31

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