Impact of maternal iron deficiency on child health
Maternal Iron Deficiency and Childhood Health- a Prospective Cohort Study
This study looks at how a lack of iron in pregnant women affects the health of their children from birth to age 7.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 6000 (estimated) |
| Sex | Female |
| Sponsor | Tampere University Hospital Academic / other |
| Locations | 1 site (Tampere, Pirkanmaa) |
| Trial ID | NCT06879080 on ClinicalTrials.gov |
What this trial studies
This observational cohort study aims to investigate the effects of maternal iron deficiency and iron deficiency anemia during pregnancy on the health outcomes of offspring. Pregnant women visiting Tampere University Hospital will be recruited to complete an online questionnaire regarding their iron status, supplementation, and any chronic conditions. The study will follow approximately 6000 mother-child pairs, tracking the health of the children from birth until the age of 7. Data will be collected from medical records to assess the impact of maternal iron levels on neonatal and childhood health.
Who should consider this trial
Good fit: Ideal candidates for this study are pregnant women who can read and write in Finnish, Swedish, or English.
Not a fit: Patients who are illiterate will not benefit from this study due to the requirement of completing an online questionnaire.
Why it matters
Potential benefit: If successful, this study could provide insights into the importance of maternal iron levels for improving pregnancy outcomes and child health.
How similar studies have performed: Other studies have shown that maternal iron status significantly affects pregnancy outcomes, suggesting that this approach is supported by existing evidence.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Pregnant * Can read and write Finnish, Swedish or English Exclusion Criteria: * Illiterate
Where this trial is running
Tampere, Pirkanmaa
- Tampere University Hospital — Tampere, Pirkanmaa, Finland (Recruiting)
Study contacts
- Study coordinator: Laura K Seppälä, MD,PhD
- Email: laura.seppala@pirha.fi
- Phone: +358444728144
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.