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Assessment of Iron Absorption From Aspergillus Oryzae

NCT03156725 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 16

Last updated 2017-05-17

No results posted yet for this study

Summary

The objective of this study was to compare the absorption of a new iron product, iron enriched Aspergillus oryzae to ferrous sulfate in humans using a double stable-isotope technique.

Conditions

  • Iron Bioavailability

Interventions

DRUG

Ferrous Sulfate

DIETARY_SUPPLEMENT

Aspiron

Sponsors & Collaborators

  • Iowa State University

    lead OTHER

Principal Investigators

  • Manju B Reddy, PhD · Iowa State University

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
SINGLE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
35 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2014-05-19
Primary Completion
2014-09-14
Completion
2016-06-04

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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 NCT03156725 on ClinicalTrials.gov