Normal Vaginal Delivery.
Conditions
Interventions
Intervention 1: The first intervention group: Two capsules contains one gram of oral Primrose oil, made by Barich Essence Company, which patients consume from night to night starts from 38 weeks to de
Sponsors
Rafsanjan University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 35 Years
Inclusion criteria
Inclusion criteria: Willingness for participant in the study Willingness to normal vaginal delivery Mother age between 18-35 years Pregnancy age: 38 weeks based on reliable first-trimester ultrasound or last menstrual period Single-fetal with a cephalic presentation based on the latest ultrasound results
Exclusion criteria
Exclusion criteria: Contraindications of primrose oil capsule Sensitivity to primrose oil capsule known history of psychological illness Delivery complications such as polyhydramnios, oligohydramnios, preeclampsia, eclampsia, vaginal bleeding History of having confirmed phsycological disorders Having any psychological disorders in the time of participation Having epilepsy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Mean Bishop score. Timepoint: It will be measured in active phase of delivery time. Method of measurement: Bishop score is obtained by scoring the five criteria of dilatation, effacement, fetal head station, softness, and cervical position during vaginal examination. Accordingly, each of the first three criteria is given a score of 0-3 and each of the following two criteria is given a score of 0-2.;The frequency of spontaneous onset of labor. Timepoint: Time of delivery. Method of measurement: Check list. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactFareeba Payhdar
Rafsanjan University of Medical Sciences
Outcome results
None listed