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Study of the Iron Absorption From Capsules Containing Lactobacilli and Iron

Not Applicable
Completed
Conditions
Healthy
Registration Number
NCT02131870
Lead Sponsor
Probi AB
Brief Summary

The purpose of this study is to study the effect of a probiotic product on iron absorption in healthy females of child-bearing age.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
Not specified
Inclusion Criteria
  • Female
  • Age ≥19 and ≤45 years
  • Hb >117g/L
Exclusion Criteria
  • Gastrointestinal diseases
  • Metabolic diseases
  • Use of other probiotic products during the study and 2 weeks before the study start
  • Pregnant or breast-feeding
  • A serum ferritin level >60 µg/L
  • Medication (oral contraceptives allowed)
  • Intake of dietary supplements (incl. iron) during the study and two weeks before the study start
  • No blood donation in the last 2 months
  • High C-reactive protein levels

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Primary Outcome Measures
NameTimeMethod
Iron absorption ratio in blood samples14 days

Iron absorption will be estimated by measuring the isotope ratio (55Fe/59Fe) in blood after addition of iron isotopes in test meals (55Fe in placebo meal, 59Fe in L plantarum DSM 9843 meal).

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Department of Internal Medicin and Clinical Nutrition, the Sahlgrenska Academy, Gothenburg University

🇸🇪

Gothenburg, Sweden

Department of Internal Medicin and Clinical Nutrition, the Sahlgrenska Academy, Gothenburg University
🇸🇪Gothenburg, Sweden

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