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Lactation Fortification Study

NCT01747668 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 89

Last updated 2013-05-31

No results posted yet for this study

Summary

To investigate the impact of nutrient supplementation during lactation on levels in breast milk.

Conditions

  • Lactation

Interventions

DIETARY_SUPPLEMENT

Similac Prenatal Vitamin soft-gel capsule

One capsule per day for Experimental Supplement A Group; Two capsules per day for Experimental Supplement B Group

DIETARY_SUPPLEMENT

Placebo (soybean oil and dl-alpha-tocopheryl acetate)

Two capsules per day for the Placebo Group; One capsule per day for the Experimental Group A

Sponsors & Collaborators

  • Abbott Nutrition

    lead INDUSTRY

Principal Investigators

  • Christina Sherry, PhD, RD · Abbott Nutrition

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-11-30
Primary Completion
2013-04-30
Completion
2013-04-30

Countries

  • United States

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 NCT01747668 on ClinicalTrials.gov