Effect of chamomile capsule in post term pregnancy
- Conditions
- post term pregnancy.Post-dates
- Registration Number
- IRCT2013062213737N1
- Lead Sponsor
- Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 70
Inclusion criterias: pregnant women 18-35 years old; Iranian nationality; have a body mass index less than 30 before pregnancy; low risk pregnancy; with getational age 41 weeks (40 weeks completely) based on LMP or ultrasound in first trimester; no history of recurrent abortion; infertility and undesirable outcomes of pregnancy; single pregnancy; cephalic presentation; alive fetus; weight of fetus between 2500-4000 gram based on physical examination or ultrasonography; cervical bishop score less than 4; intact membranous; normal pelvic according to researcher's exam; normall fetal heart rate and BPP and NST; no sensivity to herbal drugs and non-addicted persons.
Exclusion criterias: those who consume them is less than one capsule per day, more than one care session is absent, and appears allergic symptoms.
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Obstetrical outcomes. Timepoint: 2 weeks after intervention. Method of measurement: questionnair.
- Secondary Outcome Measures
Name Time Method Placental outcomes. Timepoint: During the first week of intervention and labor. Method of measurement: Observation and record in questionnaire.;Fetal outcomes. Timepoint: During first week of intervention. Method of measurement: Observation and Record questionnaire.;Maternal outcomes. Timepoint: During first week of intervention. Method of measurement: Examination, observation and record questionnaire.;Neonatal outcomes. Timepoint: To 10 days after delivery. Method of measurement: Observation and record in questionnair.