Clinical TrialID 8196
Comparative Study Among Different Doses of Ephedrine During Elective Cesarean Section Under Subarachnoid Block.
NCT05993182
Anesthesia|Cesarean Section Complications|Subarachnoid Block
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Record Fields
Scalar fields from the final clinical_trial record.
- Clinical Trial Id
- 8196
- Evidence Id
- 8196
- Core Evidence Id
- 8196
- Source Clinical Trial Id
- 8194
- Herb2 Clinical Trial Id
- HBCT008194
- Nct Id
- NCT05993182
- Title
- Comparative Study Among Different Doses of Ephedrine During Elective Cesarean Section Under Subarachnoid Block.
- Status
- Completed
- Phase
- Phase 4
- Study Result
- No
- Study Condition
- Anesthesia|Cesarean Section Complications|Subarachnoid Block
- Study Type
- Interventional
- Study Design
- Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: NONE|Primary Purpose: TREATMENT
- Intervention
- DRUG: Ephedrine 5mg|DRUG: Ephedrine 10mg|DRUG: Ephedrine 15mg
- Intervention Allocation
- Randomized
- Intervention Model
- Parallel
- Intervention Mask
- Intervention Purpose
- Treatment
- Gender
- Female
- Age
- Adult
- Enrollment
- 300
- Outcome Measure
- Survival analysis or time until an event occurs, The study time is a30 minute and blood pressure is measured automatically non invasive at 3-minute intervals. If systolic blood pressure decreased more than 20% from the baseline(Event), Intraoperatively
- Sponsor Collaborator
- Aswan University
- Funded By
- OTHER
- Location
- Aswan University, Aswan, 81511, Egypt
- Other Id
- 669/10/22
- Start Date
- 2023-08-20
- Primary Completion Date
- 2024-01-01
- Completion Date
- 2024-01-01
- First Posted
- 2023-08-15
- Results First Posted
- Last Update Posted
- 2024-03-01
- Study Document
- Study Url
- https://clinicaltrials.gov/study/NCT05993182
- Title Cn
- Title En
- Comparative Study Among Different Doses of Ephedrine During Elective Cesarean Section Under Subarachnoid Block.
- Bilingual Status
- semi_complete