A comparison of rectal and sublingual Misoprostol on Post -Partum haemorrhage during cesarean section

A comparison of rectal and sublingual Misoprostol on decreas Post -Partum haemorrhage during cesarean section

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20190204042614N1

Enrollment

Registered

2020-03-01

Start date

2018-07-23

Completion date

Unknown

Last updated

2020-03-24

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

Conditions

bleeding during and after cesarean section.

Interventions

Intervention 1: Intervention group: Rectal misoprostol is prescribed at a dose of 400 µg after spinal anesthesia. Placebo is also prescribed with rectal misoprostol. Intervention 2: Intervention group

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: Pregnant women who were candidates of Cesarean section

Exclusion criteria

Exclusion criteria: pregnancy induced hypertension twin pregnancy sensitivity to prostaglandin fetal distress

Design outcomes

Primary

Measure	Time frame
Hemoglobin before and after surgery. Timepoint: 6 hours after surgery. Method of measurement: Cell counter machine.;Hematocrit before and after surgery. Timepoint: 6 hours after surgery. Method of measurement: Cell counter machine.	—

Secondary

Measure	Time frame
Blood pressure. Timepoint: Every 5 minutes during surgery, every 15 minutes in recovery. Method of measurement: Device monitoring.;Heart beat. Timepoint: Every 5 minutes during surgery, every 15 minutes in recovery. Method of measurement: Device monitoring.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNooshin Hatamizadeh

Yazd University of Medical Sciences

n_hatamizadeh@yahoo.com+98 35 3822 4000

Outcome results

None listed

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