The effet of oral consumption of Lactuca sativa syrup on breast milk volume and weight gain of preterm infant. Preterm [premature] newborn [other]
Conditions
Interventions
Intervention 1: Intervention group: Mothers in the experimental group will receive a 240 ml Lactuca sativa syrup. In this research, 240 ml of Lactuca sativa syrup (Noma) made by Sanabel Daroo Compan
Sponsors
Iran University of Medical Sciences
Eligibility
Sex/Gender
All
Age
8 Months to 8 Months
Inclusion criteria
Inclusion criteria: have minimum 18 years old Mother's ability to read and write Have normal maternal body mass index (18/5 - 24/9 kg / m2) mothers interest to exclusive breastfeeding mothers interest to pumping breasts witt electronic pumping from third day of postpartum presence of the mother in the hospital during the study Preterm infant with gestational age less than 32 weeks Infant hospitalization in NICU fed with NG tube
Exclusion criteria
Exclusion criteria: Use of cigarette, alcohole and drugs Use of any galactagogue and complementary drug History of infertility Affiliction of mother to infectious transferable diseases from lactating such as HIV and active pulmonary tuberculosis Diabetic mother Mothers with cancer related to estrogen Mother use of anticoagulants Mother use of psychiatric drugs Breast problems such as abscesses, inverted nipples, mastitis or cancer Breast surgery Existence of congenital anomalies such as cleft palate and cleft lip Supplementation by the infant Twin or multiple infants
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Determining breast milk volume. Timepoint: Measurement of breast milk volume on days 1, 2, 3, 4, 5, 6 and 7 of the study. Method of measurement: Measurement of milk volume in mothers through sweetheart medela AND.;Determining weight gain of preterm infant. Timepoint: Measurement of preterm infant weight on day one (before intervention), day three and day seven. Method of measurement: Measurement of weight of preterm infant through a Seca scale production of Germane. | — |
Secondary
| Measure | Time frame |
|---|---|
| Pharmacological complication. Timepoint: During one week of study. Method of measurement: Mothers will notify the researcher whose telephone number is provided to the mothers if they notice any allergies or complications during the study.The researcher registers the complication in the drug side effects registration form and takes the appropriate action. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactLeila Amirifarahani
Iran University of Medical Sciences
Outcome results
None listed