Status:
TERMINATED
Norepinephrine in Caesarian Section
Lead Sponsor:
University Hospital, Antwerp
Conditions:
Cesarean Section Complications
Hemodynamic Instability
Eligibility:
FEMALE
18+ years
Phase:
PHASE4
Brief Summary
Postspinal hypotension is a frequent maternal complication in caesarian delivery under neuraxial anesthesia which is most commonly treated with the administration of phenylephrine infusion. In this tr...
Detailed Description
Patients scheduled for routine elective cesarean section under combined spinal epidural anesthesia (CSE)will be enrolled in this double-blind, randomized controlled trial, As standard of care for cesa...
Eligibility Criteria
Inclusion
- American Society of Anesthesiologists classification (ASA)1 and 2 patients
- non-laboring and singleton pregnancy
Exclusion
- patients with cardiovascular comorbidities
- any kind of cardiac and peripheral vascular disease or diabetes
- history of coagulopathy
- contra-indication to spinal anesthesia
- allergic condition to vasopressors or local anesthetics
- total body weight under 50kg or above 100kg
- length under 150cm and over 180cm Body Mass Index (BM)I ≥ 32
Key Trial Info
Start Date :
June 9 2022
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
August 27 2025
Estimated Enrollment :
11 Patients enrolled
Trial Details
Trial ID
NCT05264870
Start Date
June 9 2022
End Date
August 27 2025
Last Update
September 10 2025
Active Locations (1)
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1
Antwerp University Hospital
Edegem, Belgium, 2650