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Clinical Trials/ISRCTN61915183
ISRCTN61915183
Completed
未知

A prospective, randomized trial comparing the use of controlled limited formula (CLF) to a standard approach (SA) for efficiency and duration of breastfeeding in neonates

Institute for the Care of Mother and Child0 sites100 target enrollmentSeptember 7, 2015
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ConditionsBreastfeedingNot Applicable

Overview

Phase
未知
Intervention
Not specified
Conditions
Breastfeeding
Sponsor
Institute for the Care of Mother and Child
Enrollment
100
Status
Completed
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

2016 Results article in http://www.ncbi.nlm.nih.gov/pubmed/26918700 results

Registry
who.int
Start Date
September 7, 2015
End Date
June 1, 2015
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Institute for the Care of Mother and Child

Eligibility Criteria

Inclusion Criteria

  • •1\. Healthy term neonates with weight loss \=5 per cent between 24th and 48th hour of life
  • •2\. Singleton
  • •3\. Eutrophic with birth weight between 2500 – 4000 grams
  • •4\. Born after uncomplicated pregnancy and delivery
  • •5\. No severe congenital defects
  • •6\. Mothers are planning to breastfeed for a long time

Exclusion Criteria

  • •1\. Mother\-infant pairs with serious maternal complications (hypertension, diabetes, systemic diseases, drug abuse)
  • •2\. Mothers using therapy that might affect breastfeeding, e.g. antidepressants

Outcomes

Primary Outcomes

Not specified

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