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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04074707
Other study ID # TIPS
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date September 2019
Est. completion date December 2019

Study information

Verified date August 2019
Source Swiss Federal Institute of Technology
Contact Hanna von Siebenthal
Phone +41 44 632 53 73
Email hanna.vonsiebenthal@hest.ethz.ch
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Iron deficiency anemia (IDA) is common during pregnancy and has adverse effects on the mother, fetus and newborn. Oral iron supplements are usually recommended to prevent ID/IDA during pregnancy.

The aim of this study is to define an iron supplementation schedule with maximal absorption using serum hepcidin profiles and stable iron isotopes in pregnant women. In this randomized, open-label trial, fractional and total iron absorption will be compared from daily dosing with 60 mg iron versus alternate day and every third day dosing with 120 mg iron in pregnant Thai women with low iron stores (n=28) during their second trimester of pregnancy.

This study could have wide impact, providing the evidence base for revised, improved recommendations for iron supplementation during pregnancy.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 28
Est. completion date December 2019
Est. primary completion date December 2019
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria:

- gestational week 14-16

- singleton pregnancy

- iron depleted, defined as serum ferritin SF <30 µg/L

- non-anemic, defined as hemoglobin (Hb) >11g/dL

Exclusion Criteria:

- acute or chronic disease

- taking medications that could influence iron absorption

- smoking

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Labeled iron solution (60mg and 120mg Ferrous Sulfate)
3 doses of 60mg iron as FeSO4 are given on 3 consecutive days (e.g., days 1-3); 3 doses of 120mg iron as FeSO4 are given on one consecutive and one alternate day (e.g., days 20, 21, 23); 3 doses of 120mg iron as FeSO4 are given on one consecutive and one 3rd day (e.g., days 37, 38, 41). Iron doses are labeled with 4mg of a stable isotope in 100ml deionized water (57Fe, 58Fe or 54Fe). Participants will be randomly assigned to start with daily, alternate-day or every-third day dosing.

Locations

Country Name City State
Thailand Mahidol University Salaya Nakhon Pathom

Sponsors (2)

Lead Sponsor Collaborator
Swiss Federal Institute of Technology Mahidol University

Country where clinical trial is conducted

Thailand, 

Outcome

Type Measure Description Time frame Safety issue
Primary Fractional iron absorption in % Erythrocyte incorporation of stable iron isotopes 14 days after the last supplement intake of the consecutive day cycle Day 17
Primary Fractional iron absorption in % Erythrocyte incorporation of stable iron isotopes 14 days after the last supplement intake of the alternate day cycle Day 34
Primary Fractional iron absorption in % Erythrocyte incorporation of stable iron isotopes 14 days after the last supplement intake of the every third day cycle Day 52
Primary Total iron absorption in % Fractional iron absorption measured from consecutive day cycle multiplied by the dose Day 17
Primary Total iron absorption in % Fractional iron absorption measured from alternate day cycle multiplied by the dose Day 34
Primary Total iron absorption in % Fractional iron absorption measured from every third day cycle multiplied by the dose Day 52
Primary Serum Hepcidin in the morning a day before first supplement intake of consecutive day cycle Day 0
Primary Serum Hepcidin in the morning before first supplement intake of consecutive day cycle Day 1
Primary Serum Hepcidin in the morning before second supplement intake of consecutive day cycle Day 2
Primary Serum Hepcidin in the morning before third supplement intake of consecutive day cycle Day 3
Primary Serum Hepcidin in the morning before first supplement intake of alternate day cycle Day 17
Primary Serum Hepcidin in the morning before second supplement intake of alternate day cycle Day 18
Primary Serum Hepcidin in the morning before third supplement intake of alternate day cycle Day 20
Primary Serum Hepcidin in the morning before first supplement intake of every third day cycle Day 34
Primary Serum Hepcidin in the morning before second supplement intake of every third day cycle Day 35
Primary Serum Hepcidin in the morning before third supplement intake of every third day cycle Day 38
Primary Serum Hepcidin in the morning 14 days after last supplement intake of every third day cycle Day 52
Secondary Serum Ferritin (SF) in the morning 1 day before first supplement intake of consecutive day cycle Day 0
Secondary Serum Ferritin (SF) in the morning before first supplement intake of consecutive day cycle Day 1
Secondary Serum Ferritin (SF) in the morning before first supplement intake of alternate day cycle Day 17
Secondary Serum Ferritin (SF) in the morning before first supplement intake of every third day cycle Day 34
Secondary Serum Ferritin (SF) in the morning 14 days after last supplement intake of every third day Day 52
Secondary Hemoglobin (Hb) in the morning 1 day before first supplement intake of consecutive day cycle Day 0
Secondary Hemoglobin (Hb) in the morning before first supplement intake of consecutive day cycle Day 1
Secondary Hemoglobin (Hb) in the morning before first supplement intake of alternate day cycle Day 17
Secondary Hemoglobin (Hb) in the morning before first supplement intake of every third day cycle Day 34
Secondary Hemoglobin (Hb) in the morning 14 days after last supplement intake of every third day cycle Day 52
Secondary Soluble transferrin receptor (sTfR) in the morning 1 day before first supplement intake of consecutive day cycle Day 0
Secondary Soluble transferrin receptor (sTfR) in the morning before first supplement intake of consecutive day cycle Day 1
Secondary Soluble transferrin receptor (sTfR) in the morning before first supplement intake of alternate day cycle Day 17
Secondary Soluble transferrin receptor (sTfR) in the morning before first supplement intake of every third day cycle Day 34
Secondary Soluble transferrin receptor (sTfR) in the morning 14 days after last supplement intake of every third day cycle Day 52
Secondary C-reactive protein (CRP) in the morning 1 day before first supplement intake of consecutive day cycle Day 0
Secondary C-reactive protein (CRP) in the morning before first supplement intake of consecutive day cycle Day 1
Secondary C-reactive protein (CRP) in the morning before first supplement intake of alternate day cycle Day 17
Secondary C-reactive protein (CRP) in the morning before first supplement intake of every third day cycle Day 34
Secondary C-reactive protein (CRP) in the morning 14 days after last supplement intake of every third day cycle Day 52
Secondary Alpha-1-acid glycoprotein (AGP) in the morning 1 day before first supplement intake of consecutive day cycle Day 0
Secondary Alpha-1-acid glycoprotein (AGP) in the morning before first supplement intake of consecutive day cycle Day 1
Secondary Alpha-1-acid glycoprotein (AGP) in the morning before first supplement intake of alternate day cycle Day 17
Secondary Alpha-1-acid glycoprotein (AGP) in the morning before first supplement intake of every third day cycle Day 34
Secondary Alpha-1-acid glycoprotein (AGP) in the morning 14 days after last supplement intake of every third day cycle Day 52
Secondary Serum Hepcidin in the afternoon a day before first supplement intake of consecutive day cycle Day 0
Secondary Serum Hepcidin in the afternoon after first supplement intake of consecutive day cycle Day 1
Secondary Serum Hepcidin in the afternoon after second supplement intake of consecutive day cycle Day 2
Secondary Serum Hepcidin in the afternoon after third supplement intake of consecutive day cycle Day 3
Secondary Serum Hepcidin in the afternoon after first supplement intake of alternate day cycle Day 17
Secondary Serum Hepcidin in the afternoon after second supplement intake of alternate day cycle Day 18
Secondary Serum Hepcidin in the afternoon after third supplement intake of alternate day cycle Day 20
Secondary Serum Hepcidin in the afternoon after first supplement intake of every third day cycle Day 34
Secondary Serum Hepcidin in the afternoon after second supplement intake of every third day cycle Day 35
Secondary Serum Hepcidin in the afternoon after third supplement intake of every third day cycle Day 38
Secondary Serum Hepcidin in the afternoon 14 days after third supplement intake of every third day cycle Day 52
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