post term pregnancy. Post-dates
Conditions
Interventions
Intervention 1: Oral chamomile capsules, starting since 40 weeks of gestational age completely, primary dose of 3 capsules of 500 mg every 8 hours to do a pilot study. Intervention 2: Placebo capsules
Treatment - Drugs
Placebo
Oral chamomile capsules, starting since 40 weeks of gestational age completely, primary dose of 3 capsules of 500 mg every 8 hours to do a pilot study
Placebo capsules, containing corn starch, 500 mg
Sponsors
Tehran University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 35 Years
Inclusion criteria
Inclusion criteria: 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.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Obstetrical outcomes. Timepoint: 2 weeks after intervention. Method of measurement: questionnair. | — |
Secondary
| Measure | Time frame |
|---|---|
| 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. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactFereshte Gholami Darbarazi
Tehran university of medical science, Nursing and Midwifery school
Outcome results
None listed