Clinical TrialID 5589
Manging Post Spinal Hypotension During Elective Cesarean Section
NCT03704909
Hypotension
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Record Fields
Scalar fields from the final clinical_trial record.
- 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