Cleft breast. Cracked nipple associated with pregnancy, the puerperium, and lactation
Conditions
Interventions
Intervention 1: Intervention group: There are patients who will receive Repogen ointment before the first breastfeeding. Patients are trained in breastfeeding techniques. The use of Repogen ointment f
Sponsors
Ghoum University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
16 Years to 48 Years
Inclusion criteria
Inclusion criteria: Mothers with pregnancy over 37 weeks Mothers hospitalized for childbirth healthy mothers
Exclusion criteria
Exclusion criteria: Reluctance to cooperate he birth weight of the baby is between 2522-4222 grams Exclusive feeding with mother's milk, mother not using artificial nipples and breast milk Having a singleton pregnancy. Mothers hospitalized for childbirth
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Frequency of chest pain in the intervention and control groups. Timepoint: 3 and 7 days after using Repogen ointment. Method of measurement: Three days after delivery, face-to-face visit and seven days after delivery, by telephone, mothers and newborns in terms of the development of breast fissures, pain, bleeding, frequency of breastfeeding, use of formula, frequency of urination and baby stool. will be examined. It will be recorded in the checklist prepared by the researcher.;Severity of hernia pain in lactating women in the intervention and control groups. Timepoint: Before the first lactation and day 3 and 7 after that. Method of measurement: Three days after delivery, face-to-face visit and seven days after delivery, by telephone, mothers and newborns in terms of the development of breast fissures, pain, bleeding, frequency of breastfeeding, use ?????? ????? ?????? formula, frequency of urination and baby stool. will be examined. It will be recorded in the checklist prepared by the researcher. | — |
Secondary
| Measure | Time frame |
|---|---|
| Adequate frequency of newborns and feces of the intervention and control groups. Timepoint: Day 3 and 7 after breastfeeding. Method of measurement: based on the number of defecation cases per day.;The difference in the frequency of breastfeeding between the intervention and control groups. Timepoint: Day 3 and 7 after breastfeeding. Method of measurement: Based on the reported number of times breastfeeding.;The difference in nipple itching between the intervention and control groups is different. Timepoint: Day 3 and 7 after breastfeeding. Method of measurement: Based on questions from the patient and height in the checklist. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSeyyed Zainab Madrasi
Ghoum University of Medical Sciences
Outcome results
None listed