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Comparing of effectiveness carbetocin and oxytocin in reducing bleeding due to child delivery.

Comparison Of Carbetocin With Oxytocin In Prevention Of Postpartum Hemorrhage: A Randomized Controlled Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/10/046872
Enrollment
735
Registered
2022-10-28
Start date
Unknown
Completion date
Unknown
Last updated
2023-07-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O720- Third-stage hemorrhage

Interventions

Intervention1: Carbetocin 100 micrograms Intramuscular or Intravenous SINGLE DOSE (intravenous will be given in 500 ml of normal saline): In case of vaginal delivery, the SINGLE DOSE drug will be adm

Sponsors

Department of Obstetrics and Gynaecology
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age 18 and above Women in early spontaneous labor Women planned for cesarean section (ELECTIVE). .Women undergoing emergency cesarean section in which oxytocin stopped for more than 1hour

Exclusion criteria

Exclusion criteria: Period of gestation Women undergoing labor induction or planned for induction Underlying cardiovascular, autoimmune, hepatic, or renal disease, Placenta accreta. Known allergy to oxytocin or related product. Patient on anticoagulation. Patient not in a sound state to give consent(eclampsia, psychiatric disorders) and epilepsy disorder Instrumental delivery

Design outcomes

Primary

MeasureTime frame
The proportion of women with blood loss of at least 500 ml or the use of additional uterotonic agents at 1 hour and up to 2 hours for women who continued to bleed after 1 hour.Timepoint: 1 hour and up to 2 hours for women who continued to bleed after 1 hour.

Secondary

MeasureTime frame
1] The proportion of women with blood loss â?¥500 ml at one hour (or two hours postpartum if the bleeding continues beyond one hour) 2] Blood loss in ml at one hour (or two hours postpartum if the bleeding continues beyond one hour) 3] The proportion of women receiving additional uterotonics at one hour (or two hours postpartum if the bleeding continues beyond one hour) 4] The proportion of women receiving additional uterotonics during follow up 5] The proportion of women receiving blood transfusion during follow up 6] The proportion of women with manual removal of placenta during follow up 7] The proportion of women having additional surgical procedures Timepoint: 1 hour and up to 24 hours

Countries

India

Contacts

Public ContactDr Vishali

PGIMER, Chandigarh

vishalicool141@gmail.com9149812329

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026