Evaluation of intrauterine gel of mazo aqueous extract on postpartum hemorrhage

Phase 3

Conditions: postpartum hemorrhage.
Postpartum hemorrhage

Registration Number: IRCT20210305050583N1

Lead Sponsor: Mashhad University of Medical Sciences

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Pending

Sex: Female

Target Recruitment: 68

Inclusion Criteria

Persian has informed consent to participate in the study .
Tends to have a normal delivery.
Have a singleton pregnancy with a display of the peak of the head
Maternal body mass index is less than 30
Mathers have no history of anemia HB<7
Has no history of allergies to herbal medicines.
Has no history of medical and obstetric diseases.
Has no history of cesarean section and uterine surgery.
Has a history of giving birth less than 5 times .
Gestational age is between 37-42 weeks and in the active phase labore (4-6cm)
Fetal weight should be estimated between 2500-4000
Water bag rupture should not be more than 12 hours and temperature should not be more than 38

Exclusion Criteria

Persion dose not want to continue participating in the study.
Delivery by cesarean section.
Grade 3or 4 perineal rupture or rupture of uterus and cervix occur.
Quick deliveries.
Have delivery with the device.
Have postpartum hemorrhage more than 500cc.
Placenta out by hand

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Postpartum hemorrhage. Timepoint: At the beginning of the intervention, at the end of the first, second, third, fourth and first four hours after delivery. Method of measurement: By weighing the method of collecting blood bags and disposable drums and pads.

Secondary Outcome Measures