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The effectiveness of daily versus intermittent oral iron supplementation in pregnancy: A randomized controlled trial

Phase 4
Recruiting
Conditions
anemia in pregnancy
anemia
pregnancy
iron supplement
intermittent
iodine
Registration Number
TCTR20230310002
Lead Sponsor
Somdejprasangkharaj 17 Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
84
Inclusion Criteria

1. BMI more than 18.5
2. GA less than 20 week
3. no anemia
4. no history of thyroid disease and iodine deficiency

Exclusion Criteria

1. history of hematological disease
2. history of malabsorption and gi disease
3. history of Bariatric surgery
4. preterm labour, PPROM, sign of infection

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
hemoglobin GA 32-36 week g/dl
Secondary Outcome Measures
NameTimeMethod
iodine GA 32-36 weeks microgram/
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