The effectiveness of daily versus intermittent oral iron supplementation in pregnancy: A randomized controlled trial
Phase 4
Recruiting
- Conditions
- anemia in pregnancyanemiapregnancyiron supplementintermittentiodine
- 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
Name Time Method hemoglobin GA 32-36 week g/dl
- Secondary Outcome Measures
Name Time Method iodine GA 32-36 weeks microgram/