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Assessing the effect of Uritcadioica oral drop on postpartum hemorrhage

Assessing the effect of Uritcadioica oral drop on postpartum hemorrhage

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200620047840N1
Enrollment
100
Registered
2020-07-21
Start date
2020-07-22
Completion date
Unknown
Last updated
2020-08-17

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: After removing the placenta and membranes and stabilizing the mother's condition in terms of bleeding rate and vital signs, 10 drops of Uritcadioica in 5cc of water

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 35 Years

Inclusion criteria

Inclusion criteria: Being Iranian Persian language Without speech, hearing or mental disorders that prevents communication with others 20-35 years old Gestational age: 37-42 weeks based on the LMP or first trimester ultrasound Singleton pregnancy and cephalic presentation Gravidity = 3 Baby weight: 2,500-4,000 gr Normal length of the first, second and third stages of labor Normal amniotic fluid volume based on ultrasound (AFI: 4-25 cm) Normal vaginal delivery without using the forceps, vacuum or fundal pressure Without precipitated labor (< 3 hours) Without large episiotomy and perineal rupture (grade 3,4) Lack of chronic systemic diseases (heart disease, diabetes, hypothyroidism, coagulation disorders, anemia, preeclampsia) (by self record) Lack of cesarean section, uterine surgery or postpartum hemorrhage Without epidural or spinal anesthesia during labor and delivery Spontaneous delivery of the placenta Without excess weight (BMI= 30) Without vaginal bleeding at the second half of the current pregnancy Without previous allergies to herbal medicines (by self report) Successful breastfeeding at the first hour of childbirth

Exclusion criteria

Exclusion criteria: The mother has an allergy to Uritcadioica The mother has used other herbal or chemical medicines The mother suffers serious complications after childbirth, including heavy bleeding immediately after childbirth - high blood pressure (140/90 and above) and fever (temperature above 38 degrees) The mother has received of oxytocin more than 20 units after delivery Breastfeeding be disconnected due to maternal or neonatal reasons

Design outcomes

Primary

MeasureTime frame
The amount of postpartum hemorrhage. Timepoint: Every hour until 6 hours after delivery, then 12 and 18 and 24 hours after delivery. Method of measurement: Bleeding control is measured through a Pectorial Blood Loss Assessment Chart. Also, from all research units, 2 cc of blood is taken to measure hemoglobin and hematocrit at the beginning of admission and sent to the laboratory. 6hours after delivery, 2 cc of blood is taken from all research units to measure hemoglobin and hematocrit and will be sent to the lab.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactPadideh Janati Ataei

Shahid Beheshti University of Medical Sciences

padideh.janati@sbmu.ac.ir+98 21 8870 4816

Outcome results

None listed

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