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NCT01042561 · ClinicalTrials.gov registry record · NA

Vitamin D Status and Dose Response in Infants

A NA study, sponsored by University of Nebraska.

Completed
Registry status
NA
Development phase
64
Enrollment target

NCT01042561: Completed NA study, sponsored by University of Nebraska.

NCT01042561 is a NA study that has completed, run by University of Nebraska. The registered enrollment target is 64 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01042561, a NA study, has completed, sponsored by University of Nebraska.

COMPLETED
Registry status
NA
Development phase
64 participants
Enrollment target

Study Summary

This study will examine the relationship of serum 25(OH)D levels in infants 32 weeks and greater gestation who are fed infant formula to markers of inflammation and bone metabolism.

Primary Outcome

Total serum 25(OH)D level is currently considered the best indicator of vitamin D supply to the body from cutaneous synthesis and nutritional intake. For infants, ≤37.5 nmol/L (15 ng/mL) would be considered indicative of deficiency and \>50 nmol/L (20 ng/mL) as indicative of vitamin D sufficiency.

Interventions

  • DIETARY_SUPPLEMENT Vitamin D3
  • DIETARY_SUPPLEMENT vitamin D3 placebo

Trial Details

FieldValue
Enrollment Target 64 participants
Start Date 2009-08-07
Est. Completion 2010-08-01
Phase NA
University of Nebraska

407 total trials

What the finished NCT01042561 record still lists

NCT01042561 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 64 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower).

The record links to 0 conditions, and to 2 interventions - of which Vitamin D3 is the first listed.

NCT01042561 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01042561 about?

NCT01042561 is a clinical study titled "Vitamin D Status and Dose Response in Infants". This study will examine the relationship of serum 25(OH)D levels in infants 32 weeks and greater gestation who are fed infant formula to markers of inflammation and bone metabolism.

What is the current status of trial NCT01042561?

This trial is currently completed. It is a NA study. The enrollment target is 64 participants. The study started on 2009-08-07. Estimated completion is 2010-08-01.

What interventions are being tested in trial NCT01042561?

The interventions under investigation include: Vitamin D3 (DIETARY_SUPPLEMENT), vitamin D3 placebo (DIETARY_SUPPLEMENT).

Who is sponsoring clinical trial NCT01042561?

This trial is sponsored by University of Nebraska, which has 407 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01042561's enrollment target sits among peer trials

64 1147th of 2000 higher than 844 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA 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 NCT01042561, the US trial registry maintained by the National Library of Medicine. NCT01042561 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.