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Completed

NCT Number: NCT00109525

Early Diagnosis of Candidiasis in Premature Infants

This observational study evaluated the performance of new lab tests in detecting candida species fungal infections in extremely low birth weight (ELBW) infants quickly and accurately. 19 NICHD Neonatal Research Network sites enrolled 1,500 infants with birth weights ≤1,000g; 100 of these infants later tested positive for candidiasis. Blood, urine, and lumbar puncture samples were collected whenever other specimens were obtained from participants for cultures. These samples are being tested using the new methods and compared with standard culture results. Surviving study subjects completed a neurodevelopmental evaluation at 18-22 months corrected age.

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Key information

About this study

Candida species are a leading cause of infectious mortality in newborns with the incidence rates estimated at 4-18% in extremely low birth weight (ELBW) infants. 20-30% of these infants are likely to die. Because candida can invade virtually all body tissues (eyes, brain, heart, lung, liver, spleen, urinary tract, and joints), survivors of invasive Candida infections are at risk of blindness, developmental delays, and the need for surgical and other corrective procedures.

Time is of the essence in detecting and treating these infections, with infant mortality from candidiasis largely attributed to duration of time for cultures to become positive for Candida. Diagnosis of candidiasis is challenging - blood and urine tests are slow (taking up to 72 hours to complete) and inaccurate in many cases, showing negative results despite overwhelming disease in adults as well as children. These problems are likely made worse in neonates, with smaller amounts of blood available for testing and infections that often spread to tissues inaccessible for testing.

This observational study is evaluating the performance of new lab tests (beta-glucan assays, Gas Chromatography Mass Spectrometry for D-arabinitol, and polymerase chain reaction tests) compared to existing culture tests in detecting candida species fungal infections in extremely low birth weight (ELBW) infants quickly and accurately.

In this study, 19 NICHD Neonatal Research Network sites enrolled 1,500 infants with birth weights ≤1,000g by 72 hours of life; more than 100 of these infants later tested positive for candidiasis. In the larger cohort, whenever cultures of blood or urine were obtained, or a lumbar puncture was done, additional samples and clinical data were collected. These additional samples are being tested using the new techniques under investigation. No additional blood specimens were taken once participants had a positive blood culture for candida. Note: Test procedure reagents are being provided the Duke University laboratory by Cape Cod Incorporated and Rockeby; the Thrasher Research Fund is also providing support to the Duke University laboratory.

Surviving study subjects completed a neurodevelopmental evaluation at 18-22 months corrected age to evaluate potential early risk factors with long-term outcome.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Infants born ≤1,000g birth weight
  • Infants >72 hours old and less than 120 days old

Exclusion criteria

  • Prior positive blood culture for Candida
  • Evidence of congenital candidiasis
  • Parents/legal guardians refuse consent

Treatment and study plan

Primary outcomes

  1. Probability of invasive candidiasis based on new assay results

    Time frame: Until discharge

  2. Determine test performance of clinical predictive model

    Time frame: Until discharge

Secondary outcomes

  1. Determine test performance (sensitivity and specificity) of polymerase chain reaction (PCR) testing

    Time frame: Until discharge

  2. Determine test performance of Beta-glucan assay

    Time frame: Until discharge

  3. Determine test performance of Gas Chromatography Mass Spectrometry for D-arabinitol of blood samples

    Time frame: Until discharge

  4. Determine test performance of Gas Chromatography Mass Spectrometry for D-arabinitol of urine samples

    Time frame: Until discharge

  5. Determine test performance of the blood culture

    Time frame: Until discharge

  6. Determine test performance of the lumbar puncture (cell count, protein, glucose, and culture)

    Time frame: Until discharge

  7. Determine test performance of tracheal aspirates

    Time frame: Until discharge

  8. Determine test performance of urine cultures

    Time frame: Until discharge

  9. Compare clinical predictive model performance to neonatologist clinical judgment

    Time frame: Until discharge

  10. Determine incidence of end-organ damage in neonates with candidemia

    Time frame: Until discharge

  11. Determine resistance patterns of organisms isolated

    Time frame: Until discharge

  12. Determine molecular epidemiology of candidemia

    Time frame: Until discharge

  13. Determine genetic expression of organism virulence factors

    Time frame: Until discharge

  14. Neurodevelopmental outcome

    Time frame: 18-22 months corrected age

Sponsors and collaborators

Lead sponsor

NICHD Neonatal Research Network

Network

Collaborators

  • Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
  • National Center for Research Resources (NCRR)

Registry information

Official study title

Early Diagnosis of Nosocomial Candidiasis Study

Acronym: Candida

Important dates

Study start
2004
Primary completion
2007
Study completion
2009
First posted
Apr 29, 2005
Registry last updated
Mar 22, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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