Comparison effects of lactation induction protocol in non-pregnant mothers waiting for the birth of a baby from surrogacy according to the treatment duratio
Phase 3
- Conditions
- lactation induction in non-pregnant mothers.
- Registration Number
- IRCT20240522061869N1
- Lead Sponsor
- Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Female
- Target Recruitment
- 30
Inclusion Criteria
Non-pregnant, non-breastfeeding, and non-menopause mothers under 40 years of age who have children through surrogacy.
no history of breast surgery or other breast problems in the mother or their first-degree family.
Lack of drug interactions with the patient's medications.
No underlying diseases such as hypertension, diabetes, thrombophilia, previous thromboembolic events, migraine with aura, liver disease, and rheumatological diseases.
Absence of heart problems such as QT Prolongation.
Body Mass Index (BMI below 30).
No alcohol and tobacco use
Willingness to participate in the study and follow-ups
Exclusion Criteria
fetal congenital anomaly
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Duration and amount of milk production in three study groups. Timepoint: Monthly for up to 6 months. Method of measurement: Mother's report.
- Secondary Outcome Measures
Name Time Method Full or partial feeding of the baby with breast milk. Timepoint: Monthly for up to 6 months. Method of measurement: mother's report.;Complications. Timepoint: Monthly for up to 6 months. Method of measurement: mother's report.;The satisfaction of being a parent. Timepoint: Monthly for up to 6 months. Method of measurement: Parenting satisfaction questionnaire.