ClinicalTrials.gg
CompletedNCT07267975Updated Jun 16, 2026

Effectiveness of Oral Iron Therapy in Iron Deficiency Anemia With Daily vs Alternate Day Dosing

A Phase 3 interventional study of Ferrous sulphate and Ferrous sulphate in Iron Deficiency Anemia and Iron Deficiency Anemia Treatment, sponsored by University of Child Health Sciences and Children's Hospital, Lahore. Completed at 1 site in Pakistan. Open to participants aged 1 Day to 5 Years. Per ClinicalTrials.gov, last updated 2026-06-16.

Sponsored by University of Child Health Sciences and Children's Hospital, Lahore · Phase 3, Interventional, and Treatment

From the registry’s dates

  • Registered 10 months after the study started (first participant enrolled Jan 2025, registered Nov 2025).
Phase
Phase 3
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
1 Day to 5 Years
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-12

Among 38 studies testing ferrous sulfate in Anemia, Iron-Deficiency — 5 open to participants now, 5 under way, 1 of them phase 3. ferrous sulfate · Anemia, Iron-Deficiency.

Enrollment
21st of 37
60 · median 80
Started
2025
the only one that year
Phase 3
6 of 38
1 open now
Registered
35th of 38
by date

Among the 38 studies testing ferrous sulfate in Anemia, Iron-Deficiency, this one is the 21st largest by enrollment of the 37 interventional ones that give a count, is the only one that started in 2025, is one of 6 in phase 3, and was the 35th registered.

Anemia, Iron-Deficiency

600 studies on the registry are indexed under Anemia, Iron-Deficiency; 95 are open to participants now.

Browse Anemia, Iron-Deficiency studies →

Open to participants now

5 of the 38 studies testing ferrous sulfate in Anemia, Iron-Deficiency are open now, in 2 countries. Recruiting first, the newest first:

By country, each count listing its studies:

All 5 open studies →

About ferrous sulfate

ferrous sulfate: first FDA approval 1946 (FOLVRON). What it is approved for, and how studies give it, is on its page →

Who these studies take

Of the 54 Anemia, Iron-Deficiency studies recruiting now, 19 (35%) set no upper age limit and 31 (57%) stop at 75 or younger; 15 take children under 18; 17 take healthy volunteers.

This study: 1 Day to 5 Years · all sexes · no healthy volunteers.

The full table on the hub →

This tab as a report to print or save as PDF → With an account.

Was this useful?
Watch this landscapeDownload CSVNarrow it in search →With an account: a weekly mail of what changed among 38 studies testing ferrous sulfate in Anemia, Iron-Deficiency, or all of them as a file.
02

Study summary

Treating iron deficiency anemia in children with daily and alternate day oral iron therapy

Read the detailed description

Comparison of effectiveness of oral iron in daily and alternate group in children

03

Conditions studied

  • Iron Deficiency Anemia
  • Iron Deficiency Anemia Treatment

Keywords

  • Oral iron
  • Children
  • IDA
04

Who can participate

Ages eligible
1 Day to 5 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Patients of both genders with ages in the range of 0 -60 months suffering from IDA as per operational definition.

Exclusion criteria

Exclusion Criteria:

  1. Who have already taken treatment for IDA during last 2-months as per history/clinical record.
  2. Who have undergone recent blood transfusion during last 12-weeks as per history/clinical record.
  3. Children with chronic kidney disease, chronic liver disease, cardiac failure or concomitant
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

05

Study design

Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
60 participants (actual)

Study arms

  • Active comparator
    Continuous oral iron therapy

    Oral iron daily dosing 6mg/kg/day

    Drug: Ferrous sulphate

  • Experimental
    Intermittent oral iron

    Oral iron therapy on alternate day with dose of 6mg /kg/day for 3 mons

    Drug: Ferrous sulphate

Interventions

  • Continuous vs intermittent oral iron therapy to see the difference of Hemoglobin rose in both group

    Also known as: Daily dosing

  • Pattern of Rise in hemoglobin in alternate day doaung

    Also known as: Intermittent, alternate day dosing

06

What researchers measure

Primary outcomes

  1. Rise in hemoglobin level after oral iron

    Hemoglobin level change in g/dl

    Time frame: 3 months

  2. Change in Hemoglobin level

    Hb rise in g/dl

    Time frame: 3month

Secondary outcomes

  1. Rise in ferritin level

    Ferritin level change in ng/ml

    Time frame: 3 month

07

Study locations

1 site
  • University of child health science and the children hospital lahore
    Lahore, Punjab Province 54000, Pakistan
08

References and documents

Individual participant data

Plan to share: No — Confidentiality

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Jan 2025 to primary completion in Mar 2025, 2 months.

Of 48 phase 3 interventional studies under Anemia, Iron-Deficiency, half reached primary completion within 23 months of starting (the median), counting those still running; a quarter within 14 and three quarters within 41. This study's 2 months is below that.

How these figures are worked out, and which studies are left out of them.

Registered
Nov 24, 2025
First posted
Dec 5, 2025
StartActual
Jan 7, 2025
Primary completionActual
Mar 7, 2025
CompletionActual
May 7, 2025
Last update
Jun 16, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jun 16, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07267975
Lead sponsor
University of Child Health Sciences and Children's Hospital, Lahore
Responsible party
Marryam Kaleem (Post graduate resident, University of Child Health Sciences and Children's Hospital, Lahore) — Principal investigator
First posted
Dec 5, 2025
Start date
Jan 7, 2025
Primary completion
Mar 7, 2025
Completion
May 7, 2025
Last update
Jun 16, 2026

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jun 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Studies of the drug tested here: Ferrous sulfate

Start the discussion