The comparison of low dose with high dose of oxytocin in prevention of postpartum hemorrhage

Status

Recruiting

Phases

Phase 2

Study type

Interventional

Source

IRCT

Registry ID

IRCT20220122053780N1

Enrollment

Registered

2022-01-29

Start date

2021-12-25

Completion date

Unknown

Last updated

2022-02-07

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

Conditions

Postpartum hemorrhage. Postpartum hemorrhage

Interventions

Intervention 1: Intervention group: Receiving10 unit Oxytocin in 500 cc Ringer serum. Intervention 2: Intervention group: Receiving 60 unit Oxytocin in 500 cc Ringer serum.

Eligibility

Sex/Gender

Female

Age

18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Primiparous Age 18-45 years old Gestational age 37-41 weeks Singleton pregnancy Cephalic presentation

Exclusion criteria

Exclusion criteria: History of medical and obstetric diseases Fetal malformations Fetal weight estimate over 4000 g Diagnosis of cryoamniosis Placental abruption First and second stage of long labor Cesarean section Labor dystocia Shoulder dystocia Prenatal bleeding Instrumental labor

Design outcomes

Primary

Measure	Time frame
Postpartum hemorrhage amount. Timepoint: Immediately after delivery and each quarter to 2 hours after delivery. Method of measurement: Using measured Drape sheets for blood collection (disposable, funnelled, plastic collector bag) and reporting to cc.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Zamani

Neyshabour University of Medical Sciences

zamanim1@nums.ac.ir+98 915 154 6300

Outcome results

None listed

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