The Effect of Ovotransferrin and Lactoferrin on Iron Absorption From Ferrous Sulfate in Adult Women (OTf)
Iron-deficiency
About this trial
This is an interventional treatment trial for Iron-deficiency
Eligibility Criteria
Inclusion Criteria:
- female aged between 18-45 years old;
- SF <25 µg / L;
- BMI 18.5-24.9 kg / m2;
- weight <70 kg;
- signed informed consent;
- Able to communicate and comprehend English language.
Exclusion Criteria:
- Anemic (Hb <12 g / dL);
- inflammation (CRP> 5 mg / L);
- chronic digestive, renal and / or metabolic disease;
- chronic medications (except for oral contraceptives);
- use of vitamin, mineral and pre- and / or probiotic supplements in the previous 2 weeks and during the course of the study;
- blood transfusion, blood donation or significant blood loss over the past 4 months;
- difficulties with blood sampling;
- antibiotic treatment in the previous 4 weeks before the start of the study and during the course of the study;
- known hypersensitivity to egg;
- pregnancy (tested in serum at screening) or intention to become pregnant during the course of the study;
- lactation up to 6 weeks before study initiation;
Sites / Locations
- ETH Zurich, Laboratory of Human Nutrition
Arms of the Study
Arm 1
Arm 2
Arm 3
Other
Other
Other
OTf + FeSO4
Lf+ FeSO4
FeSO4
OTf + FeSO4 - This is the experimental arm where Ferrous sulfate will be given to the participants along with apo-Ovotransferrin, a potential iron absorption enhancer. They will be given as solutions that will be spread on bread with butter and honey, a breakfast meal.
Lf + FeSO4 - This is the experimental arm where Ferrous sulfate will be given to the participants along with lactoferrin, a potential iron absorption enhancer. They will be given as solutions that will be spread on bread with butter and honey, a breakfast meal.
FeSO4 - This is the control arm where Ferrous sulfate will be given in the form of a solution that will be spread on bread with butter and honey, as a breakfast meal