Changes in Salivary Oxytocin related to Breast Stimulation for Spontaneous Onset of Labor in Low Risk Pregnant Women: Pilot Study
Not Applicable
- Conditions
- ow risk pregnant women
- Registration Number
- JPRN-UMIN000017911
- Lead Sponsor
- St. Luke's International University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- Female
- Target Recruitment
- 15
Inclusion Criteria
Not provided
Exclusion Criteria
1. Takes medication related to gestation 2. Medical or pregnancy complications 3. Mental illness 4. Medical history of treatment of Assisted Reproductive Technology 5. BMI above 25 before pregnancy 6. Planned induced labor 7. Experienced prolonged pregnancy 8. Previous caesarian section 9. Breast feeding child
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Salivary oxytocin on 10 minutes before intervention and 15, 30, 60, 75, 90 minutes after intervention
- Secondary Outcome Measures
Name Time Method polymorphisms of oxytocin recepter