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Evaluation of intrauterine gel of mazo aqueous extract on postpartum hemorrhage

Effect Intrauterin Gel of aqueous extract of Quercus Infectoria gall on the early postpartum hemorrhage

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210305050583N1
Enrollment
68
Registered
2021-03-23
Start date
2021-05-05
Completion date
Unknown
Last updated
2021-04-26

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: In addition to receiving routine oxytocin, immediately after placenta abruption and utrerine massage an interauterine gel applicator containing 700 mg of aqueous

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
15 Years to 44 Years

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
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.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactTayebeh Mollazadeh

Mashhad University of Medical Sciences

MollazadehT982@mums.ac.ir+98 51 3859 1151

Outcome results

None listed

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