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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00754390
Other study ID # GFHNRC042
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 2005
Est. completion date May 2006

Study information

Verified date May 2018
Source USDA Grand Forks Human Nutrition Research Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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


Description:

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


Recruitment information / eligibility

Status Completed
Enrollment 17
Est. completion date May 2006
Est. primary completion date May 2006
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 21 Years to 50 Years
Eligibility Inclusion Criteria:

- Average weight for height

Exclusion Criteria:

- Medications other than birth control pills or hormone replacement therapy,

- Pregnancy within last 6 months

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Moderate Calcium, Low phytate Diet
Participants consumed diet containing 700 milligrams calcium and 440 milligrams of phytate for 4 weeks
Moderate Calcium, High Phytate Diet
Participants consumed diet containing 700 milligrams calcium and 1800 milligrams of phytate for 4 weeks
High Calcium, Low Phytate Diet
Participants consumed diet containing 1900 milligrams calcium and 440 milligrams of phytate for 4 weeks
High Calcium, High Phytate Diet
Participants consumed diet containing 1900 milligrams calcium and 1800 milligrams of phytate for 4 weeks

Locations

Country Name City State
United States United States Department of Agriculture Grand Forks Human Nutrition Research Center Grand Forks North Dakota

Sponsors (1)

Lead Sponsor Collaborator
USDA Grand Forks Human Nutrition Research Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Zinc Absorption Retention of Zinc-65 was monitored for 28 days by whole body scintillation counting. The percentage of Zinc-65 absorbed was estimated from the y-intercept of the linear portion of a semilogarithmic retention plot of percent Zinc-65 retained versus time 16 weeks
See also
  Status Clinical Trial Phase
Completed NCT05273710 - Effects of Dietary Folate and Phytate Zinc Absorption: Zinc Amino Acid Complexes vs. Zinc-chloride N/A