A comparative study on the effect of oral with vaginal of primrose oil capsule on bishap score and some prenatal outcomes
Phase 3
- Conditions
- ormal Vaginal Delivery.
- Registration Number
- IRCT20190717044248N5
- Lead Sponsor
- Rafsanjan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 105
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
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
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 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.
- Secondary Outcome Measures
Name Time Method