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Effect of Capsella Bursa Pastoris on postpartum hemorrhage

Assessing the effect of the hydro alcoholic extract of capsella bursa pastoris on postpartum hemorrhage

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016072529066N1
Enrollment
100
Registered
2016-09-04
Start date
2015-08-23
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Postpartum haemorrhage. Postpartum haemorrhage

Interventions

Intervention 1: Intervention group 1: Ten sublingual drops of hydro alcoholic extract of Capsella Bursa Pastoris( equivalent 10 grams of plant ). Intervention 2: Control group:ten sublingual drops of
Treatment - Drugs
Placebo
Intervention group 1: Ten sublingual drops of hydro alcoholic extract of Capsella Bursa Pastoris( equivalent 10 grams of plant )
Control group:ten sublingual drops of the placebo (saline 0.9 %)

Sponsors

Vice Chancellor for research of Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 35 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: The age between 20 and 35 years; the number of pregnancies less than 3; Gestational ages between 37 to 42 weeks; singleton birth with cephalic presentation; child weigh between 2500 to 4000 grams; the lack of systemic diseases (diabetes, hypothyroidism, coagulation disorders ); lack of cesarean section or uterine surgery or postpartum hemorrhage; lack of complications of pregnancy (poly hydramynus, bleeding and hypertension in pregnancy); do not use the magnesium sulfate during pregnancy; amniotic fluid is clear on during the first stage of labor; no large episiotomy during the second stage of labor (rupture of grade 3 or 4); normal during the first phase (Nulipar: 4.6 hours and up to11.7 hours, multipar: 2.4 hours and up to 5.2 hours), second (nullipar: 50 minutes and multipar: 20 minutes) and third delivery (both 30 minutes); no anemia in the mother. Exclusion criteria: Caesarean section delivery; not interested to continue to participate in the study; causing any sensitivity to the plant capsella bursa pastoris.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
A mount of bleeding. Timepoint: One hour, two hours, three hours after delivery. Method of measurement: Weighing pad and drape.;Blood presure. Timepoint: 15 minutes, 30 minutes, 45 minutes, one hour, two hours, three hours after delivery. Method of measurement: by sphygnomanometer.;Hemoglobin and hematocrit level. Timepoint: on admission and 6 hours after delivery. Method of measurement: Hemoglobin and hematocrit assessment.;Pulse. Timepoint: 15 minutes, 30 minutes, 45 minutes, one hour, two hours, three hours after delivery. Method of measurement: by counting.

Secondary

MeasureTime frame
Adverse effects. Timepoint: During Hospitalization. Method of measurement: Observation of adverse effects.;Satisfaction of Treatment. Timepoint: During Hospitalization. Method of measurement: The questions of participants.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSahar Ghalandari

School of Nursing and Midwifery of Shahid Beheshti

sghalandari68@gmail.com+98 21 8865 5366

Outcome results

None listed

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