CompletedPhase 4

Comparison of Two Norepinephrine Bolus Doses for Management of Post-spinal Hypotension During Cesarean Delivery

Egypt110 participantsStarted 2019-01-18

Plain-language summary

In this study the investigators will compare two doses of norepinephrine bolus (6 mcg and 10 mcg) in management of maternal hypotensive episode after subarachnoid block during Cesarean delivery.

Who can participate

Age range18 Years – 45 Years

SexFEMALE

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Inclusion Criteria: * Pregnant women * Scheduled for cesarean delivery Exclusion Criteria: * Patients with severe cardiac dysfunction * Patients with low blood pressure * Patients with ante-partum bleeding

What they're measuring

Rate of successful management of maternal hypotension

Timeframe: 30 minutes after spinal anesthesia

Trial details

NCT IDNCT03792906

SponsorCairo University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2019-04-25

View on ClinicalTrials.gov More Cesarean Section Complications trials