MedPath

Identifying predictors of breast milk supply following preterm birth- the PROMO study

Not Applicable
Recruiting
Conditions
actation insufficiency
Preterm birth
Lactation insufficiency
Reproductive Health and Childbirth - Breast feeding
Reproductive Health and Childbirth - Complications of newborn
Registration Number
ACTRN12621000503820
Lead Sponsor
South Australian Health and Medical Research Institute (SAHMRI)
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
200
Inclusion Criteria

Infant born <34 weeks’ gestation (i.e. up to 33+6)
-Intention to provide breast milk
-Between 0 to 168 hours (7 days) following birth
-Willing and able to comply with all study requirements
-Adequate English language skills
-Signed, written informed consent.

Exclusion Criteria

-Contraindication to breastfeeding (i.e. HIV)
-Higher order pregnancies (triplet or more)

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
© Copyright 2025. All Rights Reserved by MedPath