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The effect of Achillea millefolium on early postpartum hemorrhage

The effect of the hydro-alcoholic extract of Achillea millefolium on early postpartum hemorrhage

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20160112025983N2
Enrollment
100
Registered
2019-06-22
Start date
2019-01-20
Completion date
Unknown
Last updated
2019-08-26

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: Ten sublingual drops of hydro alcoholic extract of Achillea millefolium ( equivalent 10 grams of plant ). Intervention 2: Control group: Ten sublingual drops of pla

Sponsors

Kerman University of Medical Sciences/Deputy of research and technology
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 35 Years

Inclusion criteria

Inclusion criteria: The age between 20 and 35 years Gestational ages between 37 to 42 weeks Singleton birth with cephalic presentation child weigh between 2500 to 4000 grams Amniotic fluid is clear Normal during the first phase The number of pregnancies less than 3

Exclusion criteria

Exclusion criteria: Systemic diseases (diabetes, hypothyroidism, coagulation disorders ) Cesarean section or uterine surgery or postpartum Complications of pregnancy (poly hydramynus, bleeding and hypertension in pregnancy) Use the magnesium sulfate during pregnancy Large episiotomy during the second stage of labor

Design outcomes

Primary

MeasureTime frame
Amount of bleeding. Timepoint: One hour, two hours, three hours after delivery. Method of measurement: Weighing pad and drape.

Secondary

MeasureTime frame
Hemoglobin and hematocrit level. Timepoint: On admission and 6 hours after delivery. Method of measurement: Blood Test.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHadis Shahrahmani

Kerman University of Medical Sciences

hadis.shahrahmani@gmail.com+98 34 3132 5000

Outcome results

None listed

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