CTRI/2023/03/050468
Completed
未知
A COMPARATIVE STUDY OF SAFETY AND EFFICACY OF INTRAVENOUS CARBETOCIN VERSUS INTRAMUSCULAR CARBETOCIN INPREVENTION OF POSTPARTUM HEMORRHAGE DURING VAGINAL DELIVERY - A randomized parallel group trial.
DR SWATI TALWADE0 sites134 target enrollmentTBD
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Health Condition 1: O80- Encounter for full-term uncomplicated delivery
- Sponsor
- DR SWATI TALWADE
- Enrollment
- 134
- Status
- Completed
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\.Patient consenting for study .
- •2\.Term pregnancy (37 – 42 weeks of gestation) Expected to delivery vaginally
Exclusion Criteria
- •1\.Elective cesarean section
- •2\.Have known allergies to Carbetocin, other Oxytocin homologs or excipients in the medicinal products used in the trial;
- •3\. Have cardiovascular disorders
- •4\. Hypertensive disorders
- •5\. Have hepatic or renal disease
- •6\. Have epilepsy
- •7\. Women with coagulopathies
- •8\. Women having known conditions predisposing to atonic PPH like hydramnios,multiple gestations, and prolonged labor etc.
- •9\.Are not willing to give consent
Outcomes
Primary Outcomes
Not specified
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