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Carbetocin Versus Oxytocin for Prevention of Postcesarean Hemorrhage in Pregnancy With High Risk for PPH

R

Rajavithi Hospital

Status and phase

Completed
Early Phase 1

Conditions

Cesarean Section
High Risk Pregnancy
Postpartum Hemorrhage

Treatments

Drug: Carbetocin
Drug: oxytocin

Study type

Interventional

Funder types

Other

Identifiers

NCT04089176
T.Sopida

Details and patient eligibility

About

Objective: study efficacy of carbtocin versus oxytocin for prevention postpartum hemorrhage in high risk pregnancy who undergo cesarean section

Full description

Randomized controlled clinical trial. Defined patient in two group. Primary outcome is evaluate additional drug use Secondary outcome is evaluated estimated blood loss, hemoglobin level

Enrollment

120 patients

Sex

Female

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • previous history of postpartum hemorrhage
  • polyhydramnios
  • fetal macrosomia
  • previous cesarean section
  • grand multiparity
  • intramural myoma
  • chorioamnionitis
  • prolonged premature rupture of membrane
  • augmentation of labour

Exclusion criteria

  • pregnancy induce hypertension
  • on anticoagulant
  • placenta previa or placenta percreta

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

120 participants in 2 patient groups

protocal A
Active Comparator group
Description:
Carbetocin versus placebo
Treatment:
Drug: oxytocin
Drug: Carbetocin
protocal B
Active Comparator group
Description:
Oxytocin versus placebo
Treatment:
Drug: oxytocin
Drug: Carbetocin

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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