NCT00408980

Brief Summary

The aim of this study is to verify whether dietary manipulations in lactating women allow increasing the fat and caloric content of human milk.

Trial Health

50
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
20

participants targeted

Target at below P25 for not_applicable

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

December 7, 2006

Completed
1 day until next milestone

First Posted

Study publicly available on registry

December 8, 2006

Completed
24 days until next milestone

Study Start

First participant enrolled

January 1, 2007

Completed
Last Updated

December 8, 2006

Status Verified

November 1, 2006

First QC Date

December 7, 2006

Last Update Submit

December 7, 2006

Conditions

Breastfeeding

Keywords

dietbreast milk fat

Interventions

Fat and calorie controlled dietBEHAVIORAL

Eligibility Criteria

Age18 Years - 46 Years
Sexfemale
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • breast feeding women
  • healthy
  • on no medications

You may not qualify if:

  • women on medications

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Breast Feeding

Interventions

CD36 AntigensCaloric Restriction

Condition Hierarchy (Ancestors)

Feeding BehaviorBehavior

Intervention Hierarchy (Ancestors)

Platelet Membrane GlycoproteinsMembrane GlycoproteinsGlycoproteinsGlycoconjugatesCarbohydratesFatty Acid Transport ProteinsMembrane Transport ProteinsCarrier ProteinsProteinsAmino Acids, Peptides, and ProteinsMembrane ProteinsReceptors, Cell SurfaceReceptors, ImmunologicScavenger Receptors, Class BReceptors, ScavengerReceptors, LDLReceptors, LipoproteinDiet TherapyNutrition TherapyTherapeuticsEnergy IntakeDietNutritional Physiological PhenomenaDiet, Food, and NutritionPhysiological Phenomena

Study Officials

  • Weinstadt Morya, MD

    Shaare Zedek Medical Center, Jerusalem

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Purpose
SCREENING
Intervention Model
CROSSOVER
Sponsor Type
OTHER

Study Record Dates

First Submitted

December 7, 2006

First Posted

December 8, 2006

Study Start

January 1, 2007

Last Updated

December 8, 2006

Record last verified: 2006-11