Zinc Absorption From Zinc Citrate, Zinc Gluconate and Zinc Oxide
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ClinicalTrials.gov Identifier: NCT01576627 |
Recruitment Status :
Completed
First Posted : April 12, 2012
Last Update Posted : January 4, 2013
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Condition or disease | Intervention/treatment | Phase |
---|---|---|
Healthy | Dietary Supplement: zinc citrate Dietary Supplement: Zinc Gluconate Dietary Supplement: Zinc oxide | Not Applicable |
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 15 participants |
Allocation: | Randomized |
Intervention Model: | Crossover Assignment |
Masking: | Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor) |
Official Title: | Zinc Absorption From Zinc Supplements Comparing Zinc Citrate to Zinc Gluconate and Zinc Oxide in Young Adults |
Study Start Date : | March 2012 |
Actual Primary Completion Date : | May 2012 |
Actual Study Completion Date : | November 2012 |

Arm | Intervention/treatment |
---|---|
Experimental: zinc citrate |
Dietary Supplement: zinc citrate
10 mg of zinc as either zinc citrate |
Active Comparator: zinc gluconate |
Dietary Supplement: Zinc Gluconate
10 mg of zinc as either zinc gluconate |
Active Comparator: zinc oxide |
Dietary Supplement: Zinc oxide
10 mg of zinc as either zinc oxide |
- Fractional absorption of zinc [ Time Frame: 61 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.

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Ages Eligible for Study: | 18 Years to 45 Years (Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | Yes |
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

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01576627
Switzerland | |
ETH Zurich | |
Zurich, Switzerland, 8092 |
Responsible Party: | Prof. Michael B. Zimmermann, Prof, Swiss Federal Institute of Technology |
ClinicalTrials.gov Identifier: | NCT01576627 |
Other Study ID Numbers: |
HNL/CTC11-12 |
First Posted: | April 12, 2012 Key Record Dates |
Last Update Posted: | January 4, 2013 |
Last Verified: | January 2013 |
Zinc Zinc Oxide Trace Elements Micronutrients Physiological Effects of Drugs |
Dermatologic Agents Sunscreening Agents Radiation-Protective Agents Protective Agents |