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NCT Number: NCT00114543

Trial of Aggressive Versus Conservative Phototherapy in Infants <1,000 Grams Birth Weight

This multi-center, randomized clinical trial compared different bilirubin levels as thresholds for timing of phototherapy in extremely low birth weight infants. The primary hypothesis was that there would be no difference in death or neurodevelopmental impairment at 18-22 months corrected age in infants treated by either aggressive or conservative threshold limits. 1,978 infants were enrolled.

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Key information

About this study

In NICHD Neonatal Research Network (NRN) centers in 2002, phototherapy was administered to 94 percent of the extremely low birth weight (ELBW) infants who survive more than 12 hours. Yet, it is unclear what level of bilirubin in the blood is harmful for these very tiny infants -- no data existed from large or recent clinical trials to define the risks, benefits, and appropriate indications for phototherapy in these infants. The largest and most recent trial was the NICHD Collaborative Phototherapy Trial which involved infants treated in 1974-1976 and included only 77 ELBW infants. Data from this study and others suggested that phototherapy could have important hazards as well as benefits for ELBW infants.

This NRN study used two different bilirubin levels as thresholds for timing of phototherapy in 1,978 extremely low birth weight infants, examining the primary hypothesis that there would be no difference in death or neurodevelopmental impairment at 18-22 months corrected age between the aggressively and conservatively treated groups.

Enrolled infants were stratified by birth weight (501-750g and 751-1,000g) and randomized to receive phototherapy regimens based on either an aggressive threshold or a conservative threshold of total serum bilirubin.

In the Aggressive group:

  • 501-750 grams birth weight infants, phototherapy was started, stopped, and restarted based on a total serum bilirubin threshold level of 5 mg/dl for day of life 1-14.
  • 751-1,000 grams birth weight infants, phototherapy was started, stopped, and restarted based on a total serum bilirubin threshold level of 5 mg/dl for day of life 1-7 and 7 mg/dl for day of life 8-14.

In the Conservative group:

  • 501-750 grams birth weight infants, phototherapy was started, stopped, and restarted based on a total serum bilirubin threshold level of 8 mg/dl for day of life 1-14.
  • 751-1,000 grams birth weight infants, phototherapy was started, stopped, and restarted based on a total serum bilirubin threshold level of 10 mg/dl for day of life 1-14.

The phototherapy regimens are designed to fall within the range of clinical practice and to assure a sizable difference between groups in total serum bilirubin levels and duration of phototherapy.

The primary outcome was death or neurodevelopmental impairment at 18-22 months corrected age determined at an outpatient clinic visit. Secondary outcomes included death, abnormal neurodevelopmental outcome, severe hearing loss, cerebral palsy, blindness, and important medical outcomes.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • 501-1000 grams birth weight
  • 12-36 hours postnatal age

Exclusion criteria

  • Terminal condition (pH <6.8 for >2 hours OR persistent bradycardia, heart rate <100 bpm, associated with hypoxia for >2 hours]
  • Prior use of phototherapy
  • Major congenital anomaly
  • Hydrops fetalis or severe hemolytic disease diagnosed in-utero
  • Overt congenital nonbacterial infection
  • Parental refusal or inability to provide consent
  • Attending physician refusal
  • Parents who are considered unlikely to return for follow-up evaluation

Treatment and study plan

Aggressive Phototherapy 501-750g

Procedure

Phototherapy started, stopped, and/or restarted when total serum bilirubin levels reach 5 mg/dl during days of life 1-14.

Aggressive Phototherapy 751-1000g

Procedure

Phototherapy started, stopped, and/or restarted when total serum bilirubin levels reach 5 mg/dl during days of life 1-7, and started, stopped, and/or restarted when levels reach 7 mg/dl during days of life 8-14.

Conservative Phototherapy 501-750g

Procedure

Phototherapy started, stopped, and/or restarted when total serum bilirubin levels reach ≥8.0 mg/dl during days of life 1-14.

Conservative Phototherapy 751-1000g

Procedure

Phototherapy started, stopped, and/or restarted when total serum bilirubin levels reach ≥10.0 mg/dl during days of life 1-14.

Primary outcomes

  1. Death or neurodevelopmental impairment (MDI <70; PDI <70; cerebral palsy; blindness; or severe hearing loss)

    Time frame: 0-22 months corrected age

Secondary outcomes

  1. Patent ductus arteriosus requiring drug or surgical treatment

    Time frame: 36 weeks post conceptual age

  2. Retinopathy of prematurity

    Time frame: 36 weeks post conceptual age

  3. Bronchopulmonary dysplasia (BPD)

    Time frame: 36 weeks post conceptual age

  4. Ventilator settings and FiO2 at 36 weeks

    Time frame: 36 weeks post conceptual age

  5. Necrotizing enterocolitis (NEC)

    Time frame: 120 days old or at discharge

  6. Intraventricular hemorrhage (IVH) by grade

    Time frame: 120 days old or at discharge

  7. Periventricular leukomalacia

    Time frame: 120 days old or at discharge

  8. Sepsis

    Time frame: 120 days old or at discharge

  9. Hearing assessments

    Time frame: 120 days old or at discharge

Sponsors and collaborators

Lead sponsor

NICHD Neonatal Research Network

Network

Collaborators

  • National Center for Research Resources (NCRR)

Registry information

Official study title

A Randomized Trial of Aggressive or Conservative Phototherapy for Extremely Low Birth Weight Infants

Acronym: Phototherapy

Important dates

Study start
2002
Primary completion
2005
Study completion
2007
First posted
Jun 16, 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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