Effectiveness of Oral Iron Therapy in Iron Deficiency Anemia With Daily vs Alternate Day Dosing
Effectiveness of Intermittent Oral Iron Therapy vs Continuous Oral Iron Therapy in Treating Iron Deficiency Anemia Patients UpTo 5 Year of Age; a Randomized Control Trial
1 other identifier
interventional
60
1 country
1
Brief Summary
Treating iron deficiency anemia in children with daily and alternate day oral iron therapy
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for phase_3
Started Jan 2025
Shorter than P25 for phase_3
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 7, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 7, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
May 7, 2025
CompletedFirst Submitted
Initial submission to the registry
November 24, 2025
CompletedFirst Posted
Study publicly available on registry
December 5, 2025
CompletedDecember 5, 2025
January 1, 2025
2 months
November 24, 2025
November 24, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Rise in hemoglobin level after oral iron
Hemoglobin level change in g/dl
3 months
Change in Hemoglobin level
Hb rise in g/dl
3month
Secondary Outcomes (1)
Rise in ferritin level
3 month
Study Arms (2)
Continuous oral iron therapy
ACTIVE COMPARATOROral iron daily dosing 6mg/kg/day
Intermittent oral iron
EXPERIMENTALOral iron therapy on alternate day with dose of 6mg /kg/day for 3 mons
Interventions
Continuous vs intermittent oral iron therapy to see the difference of Hemoglobin rose in both group
Eligibility Criteria
You may qualify if:
- \- Patients of both genders with ages in the range of 0 -60 months suffering from IDA as per operational definition.
You may not qualify if:
- Who have already taken treatment for IDA during last 2-months as per history/clinical record.
- Who have undergone recent blood transfusion during last 12-weeks as per history/clinical record.
- Children with chronic kidney disease, chronic liver disease, cardiac failure or concomitant malignancy
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of child health science and the children hospital lahore
Lahore, Punjab Province, 54000, Pakistan
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- phase 3
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- PGR
Study Record Dates
First Submitted
November 24, 2025
First Posted
December 5, 2025
Study Start
January 7, 2025
Primary Completion
March 7, 2025
Study Completion
May 7, 2025
Last Updated
December 5, 2025
Record last verified: 2025-01
Data Sharing
- IPD Sharing
- Will not share
Confidentiality