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NCT03182088

Norepinephrine Infusion Different Doses in Cesarean Delivery

Completed Phase 4 Last updated 24 August 2018
What this trial tests

Phase 4 trial testing norepinephrine infusion (0.025 mcg/Kg/min) in Cesarean Section Complications in 284 participants. Completed in 30 December 2017.

Timeline
15 June 2017
Primary endpoint
25 December 2017
30 December 2017

Quick facts

Lead sponsorCairo University
PhasePhase 4
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposeprevention
Enrollment284
Start date15 June 2017
Primary completion25 December 2017
Estimated completion30 December 2017
Sites1 location across Egypt

Drugs / interventions tested

Conditions studied

Sponsor

Cairo University

Who can join

Adults 18 to 40, female only, with Cesarean Section Complications. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

three doses (0.025 mcg/Kg/min, 0.050 mcg/Kg/min, and 0.075 mcg/Kg/min) of norepinephrine will be compared for prophylaxis against Post-spinal anesthesia hypotension during Cesarean delivery.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Cesarean Section Complications

Currently open trials in the same condition.

Other Cairo University trials

Trials by the same sponsor.

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Data sources for this page

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