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NCT00136266 · ClinicalTrials.gov registry record · Phase 3

Adherence With Iron Sprinkles Among High-Risk Infants

A Phase 3 study, sponsored by Centers for Disease Control and Prevention.

Completed
Registry status
Phase 3
Development phase
128
Enrollment target

NCT00136266: Completed Phase 3 study, sponsored by Centers for Disease Control and Prevention.

NCT00136266 is a Phase 3 study that has completed, run by Centers for Disease Control and Prevention. The registered enrollment target is 128 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (83% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00136266, a Phase 3 study, has completed, sponsored by Centers for Disease Control and Prevention.

COMPLETED
Registry status
Phase 3
Development phase
128 participants
Enrollment target

Study Summary

Compared with iron drops, iron sprinkles supplied for 3 months to high-risk children beginning at age 5-7 months will increase adherence and reduce the rates of anemia and iron deficiency.

Interventions

  • DRUG Ferrous sulphate drops with vitamins A, D, and C
  • DRUG Ferrous fumarate sprinkles with vitamins and minerals

Trial Details

FieldValue
Enrollment Target 128 participants
Start Date 2005-03
Est. Completion 2005-12
Phase Phase 3

What the finished NCT00136266 record still lists

NCT00136266 is an interventional study that assigns participants to a tested intervention. The registered 128 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (83% lower).

The record links to 0 conditions, and to 2 interventions - of which Ferrous sulphate drops with vitamins A, D, and C is the first listed.

NCT00136266 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00136266 about?

NCT00136266 is a clinical study titled "Adherence With Iron Sprinkles Among High-Risk Infants". Compared with iron drops, iron sprinkles supplied for 3 months to high-risk children beginning at age 5-7 months will increase adherence and reduce the rates of anemia and iron deficiency.

What is the current status of trial NCT00136266?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 128 participants. The study started on 2005-03. Estimated completion is 2005-12.

What interventions are being tested in trial NCT00136266?

The interventions under investigation include: Ferrous sulphate drops with vitamins A, D, and C (DRUG), Ferrous fumarate sprinkles with vitamins and minerals (DRUG).

Who is sponsoring clinical trial NCT00136266?

This trial is sponsored by Centers for Disease Control and Prevention, which has 139 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00136266's enrollment target sits among peer trials

128 1601st of 2000 higher than 399 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00136266, the US trial registry maintained by the National Library of Medicine. NCT00136266 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.