Status:
COMPLETED
Iron Supplementation and Side Effects
Lead Sponsor:
Iowa State University
Conditions:
Iron Deficiency Anemia
Iron Overload
Eligibility:
FEMALE
18-40 years
Phase:
NA
Brief Summary
The objective of this study is to examine patient-reported gastrointestinal side effects, as well as iron status indicators, inflammatory markers and oxidative stress following administration of ferro...
Detailed Description
Iron deficiency anemia (IDA) afflicts more than 2 billion people globally, making it the most prevalent nutrient disorder, today. Inadequate dietary intake of iron results in consequences like cogniti...
Eligibility Criteria
Inclusion
- Age 18-40
- Female
- BMI \< 30 kg/m2
- Nonsmoker
- Non pregnant
- Non lactating
- No food allergies to wheat or dairy
- No history of gastrointestinal diseases/disorders
- Willing to discontinue use of vitamin/mineral supplements
- No medications that interfere with iron absorption
- No blood or plasma donations during study period
Exclusion
- History of gastrointestinal diseases or disorders
- Donating blood or plasma two weeks prior to study period
- On medications interfering with iron absorption
- Food allergies to wheat or dairy
- Pregnant or lactating
- Smoker
- Anemic (\< 120 g/L)
- Ferritin \> 40 ug/L
Key Trial Info
Start Date :
January 8 2018
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
April 18 2018
Estimated Enrollment :
17 Patients enrolled
Trial Details
Trial ID
NCT04018300
Start Date
January 8 2018
End Date
April 18 2018
Last Update
July 12 2019
Active Locations (1)
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1
Iowa State University
Ames, Iowa, United States, 50011