the effect of Repogen cream in preventing nipple fissures in lactating wome

Phase 3

Conditions: Cleft breast.
Cracked nipple associated with pregnancy, the puerperium, and lactation
O92.1

Registration Number: IRCT20230606058394N1

Lead Sponsor: Ghoum University of Medical Sciences

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Pending

Sex: Female

Target Recruitment: 130

Inclusion Criteria

Mothers with pregnancy over 37 weeks
Mothers hospitalized for childbirth
healthy mothers

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

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
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 Outcome Measures

Name	Time	Method
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.