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Effects of Calcium and Phytate on Zinc Absorption
This study has been completed.
Sponsored by: USDA Grand Forks Human Nutrition Research Center
Information provided by: USDA Grand Forks Human Nutrition Research Center
ClinicalTrials.gov Identifier: NCT00754390
  Purpose

This study is determine the effects of dietary calcium and phytate on zinc absorption.


Condition Intervention
Dietary Zinc Absorption
Behavioral: Moderate Ca low phytate
Behavioral: High Ca low phytate
Behavioral: Moderate Ca high phytate
Behavioral: High Ca high phytate

MedlinePlus related topics: Calcium
Drug Information available for: Calcium gluconate Phytic acid Phytate sodium
U.S. FDA Resources
Study Type: Interventional
Study Design: Prevention, Randomized, Open Label, Factorial Assignment, Bio-availability Study
Official Title: Effects of Calcium and Phytate on Zinc Absorption

Further study details as provided by USDA Grand Forks Human Nutrition Research Center:

Primary Outcome Measures:
  • Quantitative measurement of zinc absorption [ Time Frame: 4 wk ] [ Designated as safety issue: No ]

Enrollment: 17
Study Start Date: November 2005
Study Completion Date: May 2006
Primary Completion Date: May 2006 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
1: Experimental
All subjects
Behavioral: Moderate Ca low phytate
Two days of radiolabelled diet containing 700 mg Ca/d and 440 mg phytate/d
Behavioral: High Ca low phytate
Two days of radiolabelled diet containing 1900 mg Ca/d and 440 mg phytate/d
Behavioral: Moderate Ca high phytate
Two days of radiolabelled diet containing 700 mg Ca/d and 1800 mg phytate/d
Behavioral: High Ca high phytate
Two days of radiolabelled diet containing 1900 mg Ca/d and 1800 mg phytate/d

Detailed Description:

Zinc absorption is tested from 2-d of consuming each of four diets with 65Zn isotope, followed by retention monitoring in a whole body scintillation counter for 4 wks. All four 4 experimental diets are tested with each subject, in randomized order, for a total of 16 wks.

  Eligibility

Ages Eligible for Study:   21 Years to 50 Years
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Average weight for height

Exclusion Criteria:

  • Medications other than birth control pills or hormone replacement therapy,
  • Pregnancy within last 6 months
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00754390

Locations
United States, North Dakota
USDA Grand Forks Human Nutrition Research Center
Grand Forks, North Dakota, United States, 58202
Sponsors and Collaborators
USDA Grand Forks Human Nutrition Research Center
Investigators
Principal Investigator: Janet R Hunt USDA Grand Forks Human Nutrition Research Center
  More Information

Responsible Party: USDA Grand Forks Human Nutrition Research Center ( Janet R Hunt, Research Nutritiontist )
Study ID Numbers: GFHNRC042
Study First Received: September 16, 2008
Last Updated: September 17, 2008
ClinicalTrials.gov Identifier: NCT00754390  
Health Authority: United States: Federal Government

Keywords provided by USDA Grand Forks Human Nutrition Research Center:
dietary zinc absorption
dietary phytic acid
dietary calcium

Study placed in the following topic categories:
Calcium, Dietary
Zinc

ClinicalTrials.gov processed this record on January 13, 2009