General information
  • Disease category Hematologic diseases (non cancer) , Nutritional and Metabolic diseases (BASEC)
  • Recruitment status recruitment ongoing (BASEC/ICTRP)
  • Trial sites
    Zurich
    (BASEC)
  • Contact Gianno Rosalen giantizio.rosalen@hest.ethz.ch (BASEC)
  • Data Source(s) BASEC: Import from 22.08.2025 ICTRP: N/A
  • Last update 22.08.2025 10:55
HumRes65786 | SNCTP000006053 | BASEC2024-01085

Investigation of the short-term increase in serum ferritin after oral iron supplementation: An experimental study in women with iron deficiency.

  • Disease category Hematologic diseases (non cancer) , Nutritional and Metabolic diseases (BASEC)
  • Recruitment status recruitment ongoing (BASEC/ICTRP)
  • Trial sites
    Zurich
    (BASEC)
  • Contact Gianno Rosalen giantizio.rosalen@hest.ethz.ch (BASEC)
  • Data Source(s) BASEC: Import from 22.08.2025 ICTRP: N/A
  • Last update 22.08.2025 10:55

Summary description of the study

The most common biomarker for diagnosing iron deficiency is the serum or plasma concentration of the iron storage protein ferritin. In a healthy subject without inflammation or prior iron supplementation, the concentration of serum ferritin (SF) is directly proportional to the body's iron stores. The WHO recommends using SF as the primary biomarker to measure the response to iron supplementation. However, SF acutely increases immediately after oral intake of iron preparations, and this effect is likely independent of the actual total body iron stores. This effect may influence the use of SF as a biomarker during iron supplementation. If measured during or shortly after iron supplementation, this temporary increase in SF may indicate a greater benefit of oral iron supplementation than is actually the case. Furthermore, the ferritin concentration changes in inflammation, as ferritin is an acute phase protein (APP), which can further complicate the determination of iron status.

(BASEC)

Intervention under investigation

The aim of this study is to determine how long the acute increase in SF lasts before the value returns to a level that represents the actual iron stores. This is relevant as a specific SF is often targeted as a treatment goal during supplementation. Measuring SF during or shortly after iron supplementation may lead to premature cessation of supplementation before iron stores are fully replenished. Study 1: Single administration of a stable iron isotope-enriched oral iron dose: 40 mg, 100 mg, or 180 mg, depending on the study group. Assignment to study groups is done randomly. Blood samples on study days 0-7 and 14. A subgroup of the study population also receives the influenza and DTP vaccine with additional blood samples on study days 15-21 and 28. Study 2: Daily intake of oral iron for 2x30 days: 40 mg or 100 mg, depending on the study group. Assignment to study groups is done randomly. Blood samples on study days 1, 3, 6, 10, 20, 30-37, 47, 57, 67-74.

(BASEC)

Disease under investigation

Iron deficiency

(BASEC)

Criteria for participation in trial
All women who: • are aged between 18-45 years. • have a serum ferritin level below 30 µg/L. • have a body weight of up to 70 kg. • have a normal Body Mass Index (weight [kg] / (height [m])² = 18.5 – 25). • have signed the written informed consent. (BASEC)

Exclusion criteria
Women who may not participate are those who: • have a hemoglobin level below 12 g/dl (measured at the preliminary examination; for definition see page 13). • have a CRP above 5 mg/L (measured at the preliminary examination; for definition see page 13). • suffer from acute or chronic diseases that affect iron absorption and metabolism. • are on long-term medication that affects iron absorption and metabolism and intestinal physiology. • have allergies or hypersensitivities to iron preparations (ferrous fumarate, sodium dodecyl sulfate, brilliant blue FCF (E133), titanium dioxide (E171)). • have taken vitamin or mineral supplements throughout the study (since the preliminary examination). • have difficulties with blood sampling. • have had a blood transfusion, blood donation, or significant blood loss (accident, surgery) in the last 6 months. • are pregnant or breastfeeding or intend to become pregnant during the study period (approximately 1 week from the preliminary examination to the last blood sample). • abuse alcohol or drugs. • smoke (> 1 cigarette per week). • cannot follow the study requirements, e.g., due to language barriers or inability to attend a study appointment. • are study staff, their family members, employees, or other dependent persons. (BASEC)

Trial sites

Zurich

(BASEC)

not available

Sponsor

Prof. Nicole Stoffel

(BASEC)

Contact

Contact Person Switzerland

Gianno Rosalen

+41 44 655 74 16

giantizio.rosalen@hest.ethz.ch

ETH

(BASEC)

Scientific Information

not available

Name of the authorising ethics committee (for multicentre studies, only the lead committee)

Ethics Committee Zurich

(BASEC)

Date of authorisation

10.09.2024

(BASEC)


ICTRP Trial ID
not available

Official title (approved by ethics committee)
Assessing the immediate increase in serum ferritin after oral iron doses: an experimental study in iron-deficient women (INFER) (BASEC)

Academic title
not available

Public title
not available

Disease under investigation
not available

Intervention under investigation
not available

Type of trial
not available

Trial design
not available

Inclusion/Exclusion criteria
not available

not available

Primary and secondary end points
not available

not available

Registration date
not available

Incorporation of the first participant
not available

Secondary sponsors
not available

Additional contacts
not available

Secondary trial IDs
not available

Results-Individual Participant Data (IPD)
not available

Further information on the trial
not available

Results of the trial

Results summary

not available

Link to the results in the primary register

not available