Design, Implementation and Evaluation of a plan for Labor and Normal Delivery
- Conditions
- Design, Implementation and Evaluation of a plan for Labor and Normal Delivery.
- Registration Number
- IRCT20181214041963N2
- Lead Sponsor
- Ahvaz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Female
- Target Recruitment
- 256
Consent to participate in the study
primiparous women
singleton pregnancy
live fetus
maternal age 15-49 years
gestational age 37 to 42 weeks (based on the first day of the last menstrual period or first trimester ultrasound)
cephalic presentation
normal fetal heart rate (110 -160)
history of any incision on the uterus
- detection of abnormal dimensions of the pelvis through vaginal examination and examination of ischial spines, obstetric conjugation, sacrum concavity, condition of pelvic wall(s) and pubic arch angle
abnormal bleeding
epidural anesthesia
presence of any abnormalities in soft tissue or Bony birth canal (diagnosed through vaginal examination)
having an abnormal fetus or intrauterine growth restriction
indication for cesarean section (fetal distress, prolapse of the umbilical cord, diagnosis of absolute pelvic stenosis by the doctor)
known medical diseases based on the patient's file including history or current suffering from any systemic disease such as diabetes, high blood pressure, heart disease, kidney disease, nervous disease, liver disease, digestive disease, respiratory disease, thyroid disease)
Fetal membranes that have been ruptured for more than 8 hours
High-risk pregnancy (preeclampsia, placenta previa, Placental abruption, chorioamnionitis, placenta accreta)
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Type of delivery. Timepoint: after the study. Method of measurement: Questionnaire.;Satisfaction with childbirth. Timepoint: after the study. Method of measurement: Mackey questionnaire.;Childbirth Experience. Timepoint: after the study. Method of measurement: Childbirth Experience Questionnaire.;The pain of childbirth. Timepoint: During the study. Method of measurement: Visual Analogue Scale.;The length of labor stages. Timepoint: During the study. Method of measurement: Check list.;Apgar first and fifth minutes. Timepoint: After the intervention. Method of measurement: check list.;Hospitalization in the neonatal intensive care unit. Timepoint: After the intervention. Method of measurement: check list.;Postpartum bleeding. Timepoint: During the study. Method of measurement: check list.;Genital lacerations. Timepoint: During the study. Method of measurement: check list.
- Secondary Outcome Measures
Name Time Method Early breastfeeding. Timepoint: During the study. Method of measurement: check list.