Clinical TrialID 2423

Carbetocin Versus Oxytocin and Ergometrine for the Prevention of Postpartum Hemorrhage

NCT03578263

Cesarean Section Complications

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Record Fields

Scalar fields from the final clinical_trial record.

Clinical Trial Id
2423
Evidence Id
2423
Core Evidence Id
2423
Source Clinical Trial Id
2400
Herb2 Clinical Trial Id
HBCT002400
Nct Id
NCT03578263
Title
Carbetocin Versus Oxytocin and Ergometrine for the Prevention of Postpartum Hemorrhage
Status
Completed
Phase
Study Result
No
Study Condition
Cesarean Section Complications
Study Type
Interventional
Study Design
Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: SINGLE (PARTICIPANT)|Primary Purpose: PREVENTION
Intervention
DRUG: Carbetocin|DRUG: oxytocin|DRUG: ergometrine
Intervention Allocation
Randomized
Intervention Model
Parallel
Intervention Mask
Single
Intervention Purpose
Prevention
Gender
Female
Age
Adult
Enrollment
220
Outcome Measure
estimation of intraoperative blood loss (ml)., Intraoperative blood loss was measured suction bottle and the difference in weight (in grams) between the dry and the soaked operation sheets and towels (1 gram = 1 ml.). Post-operative blood loss was measured through intraperitoneal suction drain which measured every 12 hours and on removing the drain. After that, the total blood loss was calculated by the addition of intraoperative and postoperative blood loss.and vaginal bleeding, intraoperative
Sponsor Collaborator
Aswan University Hospital
Funded By
OTHER
Location
AswanUH, Aswan, 81528, Egypt
Other Id
aswu/204/2/18
Start Date
2018-04-01
Primary Completion Date
2020-03-31
Completion Date
2020-08-01
First Posted
2018-07-06
Results First Posted
Last Update Posted
2020-08-05
Study Document
Study Url
https://clinicaltrials.gov/study/NCT03578263
Title Cn
Title En
Carbetocin Versus Oxytocin and Ergometrine for the Prevention of Postpartum Hemorrhage
Bilingual Status
semi_complete