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Investigating the effect of soft capsules of ROSA Damascena on postpartum pain in multiparous women

Investigating the effect of soft capsules of ROSA Damascena on postpartum pain in multiparous women

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20231014059710N1
Enrollment
92
Registered
2024-01-05
Start date
2023-11-13
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

postpartum pain.

Interventions

Intervention 1: Intervention group: In this way, 2 hours after delivery, people in the intervention group will be given 1000 mg capsules of Rosa damascena every 8 hours to 24 hours. Capsules of1000 mg

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
15 Years to 44 Years

Inclusion criteria

Inclusion criteria: Be Iranian and be 15-44 years old Their childbirth should be natural. The gestational age should be between 37-42 weeks Live singleton baby with cephalic presentation and apparently healthy. The weight of the fetus should be 2500-4000 grams. Second to fifth birth The mother's BMI should be between 18.9-29.9. The exit of the placenta and the Fetal membranes should be automatic So have moderate or severe post partum pain. Mother's ability to breastfeed in the first 2 hours after delivery and its continuation

Exclusion criteria

Exclusion criteria: Incomplete filling of questionnaires Lack of consent to participate in the study The mother has severe bleeding. The mother should not have a difficult and long labor. Painless methods have not been used for childbirth The mother should not be addicted to narcotics or psychoactive drugs (according to the patient). The mother does not suffer from systemic diseases (diabetes, hypothyroidism, coagulation disorders) (according to the patient). There should be no interventions such as courage or use of tools (vacuum, forceps) History of cesarean section and previous pelvic surgery History of allergy to herbal medicines Have an episiotomy and grade 3 or 4 tear.

Design outcomes

Primary

MeasureTime frame
Post partum pain intensity using McGill pain ruler. Timepoint: The intensity of post-partum pain is measured before and one hour after each dose of medicine (the medicine is given to the patient every 8 hours to 24 hours (three doses). Method of measurement: Visual Analogue Scale(McGill Pain Ruler).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Mahdipoor

Shahid Beheshti University of Medical Sciences

f.mahdipoor78@gmail.com+98 21 8865 5366

Outcome results

None listed

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