Status:
COMPLETED
Comparaison of 3 Protocols of Ocytocin Administration in C Section
Lead Sponsor:
Mongi Slim Hospital
Conditions:
Cesarean Section Complications
Oxytocin Adverse Reaction
Eligibility:
FEMALE
18+ years
Phase:
NA
Brief Summary
This study aimed to compare 3 doses of ocytocin in bolus injection and contnious perfusion during C section. these doses determined by: high, intermediate and low doses, were administred to parturient...
Detailed Description
This study aimed to compare 3 doses of ocytocin in bolus injection and contnious perfusion during C section. these doses determined by: high, intermediate and low doses, were administred to parturient...
Eligibility Criteria
Inclusion
- All adult patients scheduled for C section under spinal anesthesia, monofoetal pregnancy, full term
Exclusion
- necessity of general anesthesia
- non conscent
Key Trial Info
Start Date :
September 1 2018
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
July 31 2019
Estimated Enrollment :
180 Patients enrolled
Trial Details
Trial ID
NCT04046510
Start Date
September 1 2018
End Date
July 31 2019
Last Update
August 6 2019
Active Locations (1)
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1
Mongi Slim Hospital
Tunis, Tunisia, 2046