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Effects of Vitamin A and Carotenoids on Iron Absorption

F

Federal Institute of Technology (ETH) Zurich

Status

Completed

Conditions

Iron Absorption

Treatments

Other: Labeled iron solutions

Study type

Interventional

Funder types

Other

Identifiers

NCT01493297
ETH-FeVZ

Details and patient eligibility

About

The objective of this study is to investigate the effect of vitamin A and carotenoids on iron absorption in healthy subjects with low and normal vitamin A status. Vitamin A and carotenoids have been reported to enhance the nonheme iron absorption, but the results from human isotope studies are equivocal. Radio-iron studies in Venezuelan adults have consistently reported an increase in iron absorption, whereas stable and radio isotopes studies conducted in Sweden and Switzerland reported no influence. Differences in vitamin A status of the subjects may be a possible explanation for the contradictory findings. In this study, iron absorption will be measured from an iron-fortified maize bread meal with or without retinyl palmitate or β-carotene by using both stable- and radioactive-isotope techniques in Venezuelan women with a range of vitamin A status.

Enrollment

25 patients

Sex

Female

Ages

18 to 52 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Women 18-52 years old
  • Body weight ≤ 70 kg
  • Body mass index (BMI), 18.5-30 kg/m2
  • Adequate vitamin A status (SR ≥ 0.7 μmol/L, n=20)
  • Inadequate vitamin A status (SR < 0.7 μmol/L, n=20)
  • No major medical illnesses (no known infection, gastrointestinal or metabolic disorders)

Exclusion criteria

  • Pregnancy or lactation
  • Regular intake of medication (except oral contraceptives)
  • Blood donation or significant blood loss (accident, surgery) over the past 4 months
  • Currently participating in another clinical trial or having participated in another clinical trial during the last 3 months prior to the beginning of this study
  • Former participation in a study involving administration of iron stable isotopes

Trial design

Primary purpose

Basic Science

Allocation

Non-Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

25 participants in 2 patient groups

Retinyl palmitate
Other group
Description:
Labeled iron as FeSO4 (4 mg) added to a test meal with or without retinyl palmitate (1000 RE)
Treatment:
Other: Labeled iron solutions
Beta-carotene
Other group
Description:
Labeled iron as FeSO4 (4 mg) added to a test meal with or without beta-carotene (1000 RE)
Treatment:
Other: Labeled iron solutions

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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