- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06283342
Prophylactic Iron and Nutrition in Preventing Infant Iron Deficiency
The Role of Prophylactic Iron Use and Nutrition in Preventing Iron Deficiency in Infancy
Study Overview
Status
Detailed Description
Iron plays an important role in oxidation and reduction reactions, which have a very important place in the continuation of life. Iron plays an essential role in these reactions because it can easily gain and lose electrons in redox reactions. Iron is mostly found in the heme molecule in organisms. However, iron has structural and functional importance for many enzymes and proteins other than heme. Iron deficiency (ID) is the most common nutritional deficiency in children worldwide. ID is more common in socio-economically developing geographies. However, it is still an important problem in developed countries. A plasma ferritin level below 12 mg/L is defined as ID, which is often used synonymously with iron deficiency anemia (IDA). However, ID develops before anemia occurs. Weakness, fatigue, tiring quickly, insomnia, and regression in neuro-cognitive functions may occur in ID that precedes the signs of anemia. With the development of anemia, the clinical diagnosis of IDA is fully revealed.
In ID that occurs in infancy, psychomotor development is adversely affected, and the development of cognitive functions slows down or even stops. Immune system functions regress. Although iron treatment can reverse these negative effects, some effects are permanent. Therefore, prevention of ID is more important than treatment. In addition, it is easier and cheaper to prevent ID and IDA than to treat them. It is a health policy to recommend iron prophylaxis to children aged 4-12 months in the Republic of Turkey.
Adding iron-rich foods to the diet, adequate breast milk intake, and prophylaxis with iron preparations can be used to prevent ID and IDA. However, there are different data in the literature on the use of prophylactic iron preparations.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Konya, Turkey, 42090
- Konya Training and Research Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Patients aged between 6-24 months and admitted to the general pediatrics outpatient clinic
Exclusion Criteria:
- Chronic disease
- Blood transfusion history,
- Thalassemia carrier status
- Clinical diagnosis of infection or elevated C-reactive protein (CRP)
- Patients who received iron deficiency or iron deficiency anemia treatment
- Those who were born prematurely
- Patients with low birth weight
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Iron deficiency group
Patients with a ferritin level below 12 mg/L were considered to have Iron deficiency group.
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Not iron deficiency group
Patients with a ferritin level above 12 mg/L were considered to have not iron deficiency group.
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Iron deficiency anemia group
Patients with ferritin level below 12 mg/L and hemoglobin (Hb) value below 11 g/dL were considered to have IDA.
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Not iron deficiency anemia group
Patients with ferritin level below 12 mg/L and hemoglobin (Hb) value above 11 g/dL were considered to have Not iron deficiency anemia group.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Ferritine level
Time Frame: day 1
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Ferritin level below 12 mg/L was considered iron deficiency.
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day 1
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Hemoglobin level
Time Frame: day 1
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Hemoglobin (Hb) values below 11 g/dL were considered as having anemia
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day 1
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Prophylactic iron use rate
Time Frame: 15 days
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Giving 10 mg/day iron drops to babies starting from the 4th month was considered as the correct prophylaxis recommendation.
Prophylactic iron use rates were calculated by dividing those using iron prophylaxis in all groups by the number of participants in the groups.
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15 days
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Iron-sufficient supplementary food intake rate of babies
Time Frame: 15 days
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Babies whose mothers answered "yes" to at least two of the following questions in the survey evaluating babies' iron-sufficient supplementary food intake were considered to be fed adequately in terms of iron:
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15 days
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Breast milk usage rate
Time Frame: 15 days
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Exclusive breastfeeding for at least 6 months after birth was considered adequate breast milk intake.
Those who breastfed during this period were considered to have used sufficient breast milk.
The breast milk usage rate was found by dividing those who received adequate breast milk by the participants in the group.
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15 days
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Konya Pediatric Hematology
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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