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Completed Phase 1 Interventional Accepts healthy volunteers

Vitamin E for Extremely Preterm Infants

ClinicalTrials.gov ID: NCT01193270

Public ClinicalTrials.gov record NCT01193270. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 2:45 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Single-Dose Vitamin E for Prevention of Mortality and Morbidity in Extremely Preterm Infants: Pilot Study

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this pilot trial is to test the safety and efficacy of administering one dose of vitamin E, via a tube into the stomach, to extremely preterm infants (less than 27 weeks gestation and less than 1000 grams birth weight). This pilot will examine whether a single dose of vitamin E will be absorbed into the infants' bloodstreams with resulting serum α-tocopherol level in the target range of 1-3 mg/dl.

Study identification

NCT ID
NCT01193270
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Enrollment
93 participants

Conditions and interventions

Eligibility (public fields only)

Age range
Up to 4 Hours
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 2010 (Type not available)
Primary completion
Aug 2011 (Actual)
Completion
Aug 2011 (Actual)
Last update posted
Nov 11, 2015

2010 – 2011

United States locations

U.S. sites
16
U.S. states
14
U.S. cities
15
Facility City State ZIP Site status
University of Alabama at Birmingham Birmingham Alabama 35233 —
Stanford University Palo Alto California 94304 —
Yale University New Haven Connecticut 06504 —
Emory University Atlanta Georgia 30303 —
Indiana University Indianapolis Indiana 46202 —
University of Iowa Iowa City Iowa 52242 —
Tufts Medical Center Boston Massachusetts 02111 —
Wayne State University Detroit Michigan 48201 —
University of New Mexico Albuquerque New Mexico 87131 —
RTI International Durham North Carolina 27705 —
Duke University Durham North Carolina 27710 —
Case Western Reserve University, Rainbow Babies and Children's Hospital Cleveland Ohio 44106 —
Brown University, Women & Infants Hospital of Rhode Island Providence Rhode Island 02905 —
University of Texas Southwestern Medical Center at Dallas Dallas Texas 75235 —
University of Texas Health Science Center at Houston Houston Texas 77030 —
University of Utah Salt Lake City Utah 84108 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01193270, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 11, 2015 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01193270 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →