Investigating the effect of soft capsules of ROSA Damascena on postpartum pain in multiparous wome
- Conditions
- postpartum pain.
- Registration Number
- IRCT20231014059710N1
- Lead Sponsor
- Shahid Beheshti University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 92
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
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.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 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).
- Secondary Outcome Measures
Name Time Method