Status:
COMPLETED
Comparison of Two Norepinephrine Bolus Doses for Management of Post-spinal Hypotension During Cesarean Delivery
Lead Sponsor:
Cairo University
Conditions:
Cesarean Section Complications
Spinal Anesthetic Toxicity
Eligibility:
FEMALE
18-45 years
Phase:
PHASE4
Brief 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.
Detailed Description
Maternal hypotension after subarachnoid block is a frequent and deleterious complication during cesarean delivery. Although prophylaxis against hypotension using vasopressors had become a standard rec...
Eligibility Criteria
Inclusion
- Pregnant women
- Scheduled for cesarean delivery
Exclusion
- Patients with severe cardiac dysfunction
- Patients with low blood pressure
- Patients with ante-partum bleeding
Key Trial Info
Start Date :
January 18 2019
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
May 1 2019
Estimated Enrollment :
110 Patients enrolled
Trial Details
Trial ID
NCT03792906
Start Date
January 18 2019
End Date
May 1 2019
Last Update
September 24 2021
Active Locations (1)
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1
Ahmed Mohamed Hasanin
Cairo, Egypt, 11432