Questionnaire About Risk Factors of Iron Deficiency Anemia in Pregnancy
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Iron Deficiency Anaemia. Basic parameters: 18 years — 45 years · Female.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Questionnaire About Risk Factors of Iron Deficiency Anemia in Pregnancy and How to Prevent it
Overview
Anemia in pregnancy,and especially iron deficiency anemia is both a long standing scholarly interest ,the aim of my research to summarise the risk factors of iron deficiency anemia in pregnancy, especially in Egypt as a less developed country,and suggest recommendations about how to prevent it
Primary outcome measures
- Risk factors of iron deficiency anemia in pregnancy [Time frame: 1 Year]
Eligibility criteria
Inclusion criteria
- Women aged 18 years or older with established iron deficiency anemia (HB less than 10)
- established intrauterine pregnancy
- women want to participate in the study
Exclusion criteria
- anemia due to other causes
- recent blood transfusion in the last 3 months
- women with threatened miscarriage
- women are known to have pathological blood loss (urinary bleeding or GIT bleeding) 5- history of haematological disorder 6- women used iron in the past 3 months
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Study design
- Observational model
- Cohort
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT06761352 · Iron deficiency anemia in preg