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Comparison of the effect of nipple stimulation with syntocinon drug on the induction of labour

Phase 2
Conditions
labour induction.
Failed induction of labour
Registration Number
IRCT2013112515544N1
Lead Sponsor
Vice chancellor for research,Nursing & Midwifery Faculty of Shahid Beheshty University of Medical Sc
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
140
Inclusion Criteria

age of18-35 years old, gestational age of 38-42 weeks based on LMP or ultrasound before 26 weeks? requiring termination of pregnancy for fetal or maternal indications? nulliparous wemon? single fetous with cephalic presentation? intact membrane? bishop score< 4? body mass index between 20 to 30? estimated fetal weight between ( 4500-2500 gr )? lack of any kind of diseases and high risk pregnancy? not use of any kind of chemical drug or herb to start labour for 48 hours before admission? lack of any problems (eg, tumor) in the breast.
Exclusion criteria: Incidence of each type of obstetric emergencies (such as cord prolapse )? discontinuing of the study by patient request ?spontaneous rupture of membrane before 4-5cm dilatation.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Bishop score. Timepoint: every2 hours during first stage of labour. Method of measurement: by vaginal examination.
Secondary Outcome Measures
NameTimeMethod
Abnormal fetal heart rate. Timepoint: During the study. Method of measurement: Fetel monitoring device.;Apgar score. Timepoint: 1&5 minute after delivery. Method of measurement: Apgar scoring System.;Pain intensity. Timepoint: During the study. Method of measurement: Mcgill ruler.;Lenght of the first and second stages of labor. Timepoint: End of delivery. Method of measurement: minute.
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