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NCT05459298 · ClinicalTrials.gov registry record · NA

ViDES Trial (Vitamin D Extra Supplementation)

A NA study of Vitamin D Deficiency, sponsored by The University of Texas Health Science Center, Houston.

Active
Registry status
NA
Development phase
180
Enrollment target
1
Study location

NCT05459298 is a NA study of Vitamin D Deficiency that is active but no longer recruiting, run by The University of Texas Health Science Center, Houston. The registered enrollment target is 180 participants, below the 272-participant average among 48 other Vitamin D Deficiency trials with a reported enrollment target (34% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT05459298, a NA study of Vitamin D Deficiency, is active but no longer recruiting, sponsored by The University of Texas Health Science Center, Houston.

ACTIVE NOT RECRUITING
Registry status
NA
Development phase
180 participants
Enrollment target
1
Study location

Study Summary

The objective of the study is to compare supplementation with vitamin D at 800 IU/day to usual care for the first 28 days after birth with respect to 25 (OH) vitamin D levels and indicators of likely or plausible effects of vitamin D supplementation on the function or structure of the lung, bones, immune system, and brain in extremely premature (EP) infants who are \<28 weeks gestational age (GA) or \<1000 grams of birth weight (BW). The study results will be analyzed as intention to treat Bayesian analyses (Frequentist analyses will also be performed).

Conditions Studied

Interventions

  • DIETARY_SUPPLEMENT Placebo
  • OTHER Usual Care
  • DIETARY_SUPPLEMENT 800 IU/day vitamin D supplementation with feedings in the first 28 days after birth

Study Locations (1)

Texas

  • The University of Texas Health Science Center at Houston - Houston

Trial Details

FieldValue
Enrollment Target 180 participants
Start Date 2022-09-06
Est. Completion 2027-12-01
Phase NA

What the Registry Record Tells You About NCT05459298

The ClinicalTrials.gov registry entry for NCT05459298 describes a study currently listed as active not recruiting, categorized as NA. The registered enrollment target is 180 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 272-participant average among 48 other Vitamin D Deficiency trials with a reported enrollment target (34% lower). The listed sponsor is The University of Texas Health Science Center, Houston, which has 732 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Vitamin D Deficiency appearing as the primary indexed condition, and to 3 interventions - of which Placebo is the first listed.

NCT05459298 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.

Frequently Asked Questions

What is clinical trial NCT05459298 about?

NCT05459298 is a clinical study titled "ViDES Trial (Vitamin D Extra Supplementation)". The objective of the study is to compare supplementation with vitamin D at 800 IU/day to usual care for the first 28 days after birth with respect to 25 (OH) vitamin D levels and indicators of likely or plausible effects of vitamin D supplementation on the function or structure of the lung, bones, i...

What is the current status of trial NCT05459298?

This trial is currently active not recruiting. It is a NA study. The enrollment target is 180 participants. The study started on 2022-09-06. Estimated completion is 2027-12-01.

What conditions does trial NCT05459298 study?

This clinical trial studies the following conditions: Vitamin D Deficiency.

What interventions are being tested in trial NCT05459298?

The interventions under investigation include: Placebo (DIETARY_SUPPLEMENT), Usual Care (OTHER), 800 IU/day vitamin D supplementation with feedings in the first 28 days after birth (DIETARY_SUPPLEMENT).

Who is sponsoring clinical trial NCT05459298?

This trial is sponsored by The University of Texas Health Science Center, Houston, which has 732 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05459298 being conducted?

This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.