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Zinc Absorption From Zinc Citrate, Zinc Gluconate and Zinc Oxide

Not Applicable
Completed
Conditions
Healthy
Interventions
Dietary Supplement: Zinc oxide
Dietary Supplement: zinc citrate
Dietary Supplement: Zinc Gluconate
Registration Number
NCT01576627
Lead Sponsor
Prof. Michael B. Zimmermann
Brief Summary

The goal of this trial is to evaluate zinc citrate, a zinc compound with promising sensory properties and a high zinc content, as an alternative zinc compound to be used for supplementation or food fortification. The bioavailability of zinc citrate given as a supplement to young Swiss adults will be assessed and compared to the bioavailability of the commonly used zinc compounds zinc gluconate and zinc oxide.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
15
Inclusion Criteria
  • Male or female of 18 to 45 years old
  • Body Mass Index in the range of 19 to 25
  • No mineral and vitamin supplements two weeks prior to the study and during the whole duration of the study
Exclusion Criteria
  • Any metabolic, gastrointestinal or chronic disease (according to the subjects own statement)
  • Long-term medication during the whole study (except for contraceptives)
  • Vegans
  • Pregnancy
  • Lactation
  • Intention to become pregnant during the course of the study
  • Lack of safe contraception
  • Consumption of mineral and vitamin supplements within 2 weeks prior to 1st test supplement administration
  • Earlier participation in any nutrition study using Zn stable isotopes as well as participation in any other clinical study within the last 30 days and during this study

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
zinc oxideZinc oxide-
zinc citratezinc citrate-
zinc gluconateZinc Gluconate-
Primary Outcome Measures
NameTimeMethod
Fractional absorption of zinc61 days

Fractional absorption of zinc is estimated by using the double isotope tracer ratio technique by administering 67Zn as oral and 70Zn as intravenous stable isotopes.The urinary enrichment with both isotopes is measured in a spot urine sample by inductively coupled plasma mass spectrometry.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

ETH Zurich

🇨🇭

Zurich, Switzerland

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