Status:

COMPLETED

Vasopressor Prophylaxis After Spinal Anesthesia

Lead Sponsor:

Cairo University

Conditions:

Cesarean Section Complications

Eligibility:

FEMALE

18-40 years

Phase:

PHASE4

Brief Summary

Norepinephrine has been recently introduced as a prophylactic vasopressor during Cesarean delivery with promising results ; However, the optimum dose for efficient prophylaxis with the least side effe...

Detailed Description

Maternal hypotension is a common complication after spinal anesthesia for cesarean delivery (CD). Using vasopressors have been considered a gold standard for prevention of post-spinal hypotension (PSH...

Eligibility Criteria

Inclusion

  • full term singleton pregnant women
  • Scheduled for elective Cesarean Delivery
  • Aged between 18 and 40 years

Exclusion

  • Cardiac morbidities
  • Hypertensive disorders of pregnancy,
  • Peripartum bleeding
  • Baseline systolic blood pressure (SBP) \< 100 mmHg
  • Body mass index \> 35

Key Trial Info

Start Date :

August 2 2017

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

December 10 2018

Estimated Enrollment :

270 Patients enrolled

Trial Details

Trial ID

NCT03234816

Start Date

August 2 2017

End Date

December 10 2018

Last Update

January 15 2019

Active Locations (1)

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1

Cairo University

Cairo, Egypt