Clinical TrialID 5589

Manging Post Spinal Hypotension During Elective Cesarean Section

NCT03704909

Hypotension

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Trial: 1Ingredient: 1Links: 1
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Record Fields

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Clinical Trial Id
5589
Evidence Id
5589
Core Evidence Id
5589
Source Clinical Trial Id
5574
Herb2 Clinical Trial Id
HBCT005574
Nct Id
NCT03704909
Title
Manging Post Spinal Hypotension During Elective Cesarean Section
Status
Completed
Phase
Phase 4
Study Result
No
Study Condition
Hypotension
Study Type
Interventional
Study Design
Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: TRIPLE (PARTICIPANT, CARE_PROVIDER, INVESTIGATOR)|Primary Purpose: PREVENTION
Intervention
DRUG: Adrenaline|DRUG: Ephedrine
Intervention Allocation
Randomized
Intervention Model
Parallel
Intervention Mask
Triple
Intervention Purpose
Prevention
Gender
Female
Age
Adult
Enrollment
143
Outcome Measure
delta SBP (D), difference between baseline and the lowest systolic blood pressure., at the end of intrathecal injection until delivery|delta MBP (D), difference between baseline and the lowest mean blood pressure., at the end of intrathecal injection until delivery
Sponsor Collaborator
Ben marzouk Sofiene
Funded By
OTHER
Location
Tunis maternity and neonatology center,, Tunis, 1007, Tunisia
Other Id
Adrenaline
Start Date
2018-09-01
Primary Completion Date
2018-12-31
Completion Date
2018-12-31
First Posted
2018-10-15
Results First Posted
Last Update Posted
2019-03-13
Study Document
Study Url
https://clinicaltrials.gov/study/NCT03704909
Title Cn
Title En
Manging Post Spinal Hypotension During Elective Cesarean Section
Bilingual Status
semi_complete