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A Post Breastfeeding Follow-Up Study

NCT02913638 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 196

Last updated 2017-02-13

No results posted yet for this study

Summary

The purpose of this clinical study which is to evaluate the benefits of lactation support intervention, in conjunction with maternal nutritional supplementation during the last trimester to 12 weeks postpartum in comparison to pre- and postnatal care on 1) breast feeding practices (primary objective), and 2) cognitive development in children within 28 months 16 days - 32 months 30 days (secondary objective).

Conditions

  • Breast Feeding

Sponsors & Collaborators

  • Abbott Nutrition

    lead INDUSTRY

Principal Investigators

  • Dieu Huynh, M.D. · Abbott Nutrition

Eligibility

Min Age
28 Months
Max Age
32 Months
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-09-30
Primary Completion
2016-12-31
Completion
2016-12-31

Countries

  • Vietnam

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02913638 on ClinicalTrials.gov