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Completed Phase 3 Interventional Results available

Fluconazole Prophylaxis for the Prevention of Candidiasis in Infants Less Than 750 Grams Birthweight

ClinicalTrials.gov ID: NCT00734539

Public ClinicalTrials.gov record NCT00734539. 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 Sep 3, 2026, 5:02 AM EDT

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

Official title

Fluconazole Prophylaxis for the Prevention of Candidiasis in Infants < 750 Grams Birth

Brief summary

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

The most common etiology of infection-related death or neurodevelopmental impairment in neonates with birthweight \<750 g is invasive candidiasis. Over 70% of the premature neonates who develop invasive candidiasis will die or suffer severe, permanent neurologic impairment. Fluconazole has been commonly used off-label in the neonatal intensive care unit, but definitive recommendations for its use in the nursery have been hampered by the limited number of well-designed trials. In neonates weighing \<750 g, appropriate dosing is not known, definitive safety and long-term follow up trials have not been completed, and there have not been well-powered trials conducted to establish the efficacy of the product using mortality as part of the primary endpoint. Three recent proof-of-concept studies suggest that fluconazole will be safe and effective, and a recently completed pharmacokinetic study is providing data to give preliminary dosing guidance. The next logical step in drug development is proposed by this research: to conduct a pivotal trial to determine the safety and efficacy of fluconazole in premature neonates with 2-year neurodevelopmental follow-up assessment. 362 neonates, with a birthweight \<750g, were randomized at 33 US centers, to twice weekly fluconazole (6 mg/kg) or placebo for the first 6 weeks of life. The primary efficacy endpoint will be Candida-free survival at study day 49. The research will establish definitive dosing, safety, and efficacy of fluconazole; it will also provide critical information on the effects of fluconazole on neurodevelopmental impairment and antifungal resistance. Potential Impact: Approximately 17,000 neonates are born \<750 grams each year in the United States. Over 5000 will die or develop invasive Candida infections. Demonstrating safety and efficacy of fluconazole in preterm neonates will improve the survivability and long term outcomes for these neonates.

Study identification

NCT ID
NCT00734539
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Daniel Benjamin
Other
Enrollment
362 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
2 Days to 5 Days
Sex
All
Healthy volunteers
Healthy volunteers not accepted

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

Study timeline

Start date
Oct 31, 2008
Primary completion
Nov 30, 2011
Completion
Mar 31, 2013
Last update posted
Feb 28, 2019

2008 – 2013

United States locations

U.S. sites
33
U.S. states
19
U.S. cities
28
Facility City State ZIP Site status
University of Alabama at Birmingham Birmingham Alabama 35233
University of Arkansas for Medical Sciences Little Rock Arkansas 72202
Arkansas Childrens Hospital Little Rock Arkansas 72205
Children's Hospital of Orange County Orange California 92868
University of California-San Diego San Diego California 92103
University of Florida Gainesville Florida 32610
Baptist Medical Center Jacksonville Florida 32209
Shands Jacksonville Medical Center Jacksonville Florida 32209
University of Miami Miami Florida 33136
Riley Hospital Indianapolis Indiana 46601
Memorial Hospital South Bend Indiana 46601
Wesley Medical Center Wichita Kansas 67214
Kosair Children's Hospital Louisville Kentucky 40202
Tulane University School of Medicine New Orleans Louisiana 70112
Wayne State University Detroit Michigan 48201
University of Minnesota, Fairview Medical Center Minneapolis Minnesota 55455
University of Nevada School of Medicine Las Vegas Nevada 89109
West Jersey Hospital - Voorhees Voorhees Township New Jersey 08043
Brookdale University Medical Center Brooklyn New York 11203
Kings County Hospital Center Brooklyn New York 11203
SUNY Dowstate Medical Center Brooklyn New York 11203
Columbia University Medical Center New York New York 10032
Duke University Medical Center Durham North Carolina 27705
Pitt County Memorial Hospital Greenville North Carolina 27834
Akron Children's Hospital Akron Ohio 44313
Oregon Health Sciences Center Portland Oregon 97201
Pennsylvania Hospital Philadelphia Pennsylvania 19107
University of Tennessee Memphis Tennessee 38130
Parkland Memorial Hospital Dallas Texas 75235
Cooks Children's Medical Center Fort Worth Texas 76104
University of Texas Medical Branch Galveston Texas 77555
Texas Children's Hospital/Baylor College of Medicine Houston Texas 77030
University of Texas - Houston Houston Texas 77030

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 NCT00734539, 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 Feb 28, 2019 · Synced Sep 3, 2026

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The complete protocol, eligibility criteria, and contact information for NCT00734539 live on ClinicalTrials.gov.

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