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Early Diagnosis of Candidiasis in Premature Infants (Candida)

N

NICHD Neonatal Research Network

Status

Completed

Conditions

Infection
Infant, Low Birth Weight
Infant, Newborn
Candidiasis
Candida
Infant, Small for Gestational Age
Infant, Premature

Study type

Observational

Funder types

NETWORK
NIH

Identifiers

NCT00109525
U10HD053109 (U.S. NIH Grant/Contract)
M01RR016587 (U.S. NIH Grant/Contract)
M01RR000032 (U.S. NIH Grant/Contract)
M01RR006022 (U.S. NIH Grant/Contract)
U10HD021364 (U.S. NIH Grant/Contract)
U10HD027880 (U.S. NIH Grant/Contract)
U10HD027856 (U.S. NIH Grant/Contract)
U10HD036790 (U.S. NIH Grant/Contract)
U10HD053089 (U.S. NIH Grant/Contract)
U10HD027851 (U.S. NIH Grant/Contract)
U10HD040689 (U.S. NIH Grant/Contract)
M01RR000039 (U.S. NIH Grant/Contract)
M01RR008084 (U.S. NIH Grant/Contract)
U10HD027871 (U.S. NIH Grant/Contract)
M01RR000059 (U.S. NIH Grant/Contract)
UL1RR024139 (U.S. NIH Grant/Contract)
U10HD021373 (U.S. NIH Grant/Contract)
M01RR000997 (U.S. NIH Grant/Contract)
M01RR000080 (U.S. NIH Grant/Contract)
U10HD027853 (U.S. NIH Grant/Contract)
M01RR000044 (U.S. NIH Grant/Contract)
U10HD053119 (U.S. NIH Grant/Contract)
M01RR000070 (U.S. NIH Grant/Contract)
U10HD040521 (U.S. NIH Grant/Contract)
NICHD-NRN-0030
UL1RR024160 (U.S. NIH Grant/Contract)
U10HD040498 (U.S. NIH Grant/Contract)
M01RR000633 (U.S. NIH Grant/Contract)
U10HD040492 (U.S. NIH Grant/Contract)
M01RR007122 (U.S. NIH Grant/Contract)
M01RR000030 (U.S. NIH Grant/Contract)
M01RR000750 (U.S. NIH Grant/Contract)
U10HD021397 (U.S. NIH Grant/Contract)
U10HD034216 (U.S. NIH Grant/Contract)
M01RR000054 (U.S. NIH Grant/Contract)
U10HD021385 (U.S. NIH Grant/Contract)
U10HD027904 (U.S. NIH Grant/Contract)
U10HD040461 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

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.

Full description

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.

Enrollment

1,500 patients

Sex

All

Ages

3 to 120 days old

Volunteers

Accepts Healthy Volunteers

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

Trial contacts and locations

20

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Data sourced from clinicaltrials.gov

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