Skip to main content
OpenTrials
Recruiting

NCT Number: NCT05347238

Dopamine vs. Norepinephrine for Hypotension in Very Preterm Infants With Late-onset Sepsis

Fluid-unresponsive hypotension needing cardiotropic drug treatment is a serious complication in very preterm neonates with suspected late-onset sepsis (LOS; defined as culture positive or negative bloodstream infection or necrotizing enterocolitis occurring >48 hours of age). In Canada, ~250 very preterm neonates receive cardiotropic drugs for LOS related fluid-unresponsive hypotension every year; of these ~35-40% die. Unlike for adult patients, there is little evidence to inform practice. While several medications are used by clinicians, the most frequently used medications are Dopamine (DA) and Norepinephrine (NE). However, their relative impact on patient outcomes and safety is not known resulting in significant uncertainty and inter- and intra-unit variability in practice. Conducting large randomized trials in this subpopulation can be operationally challenging and expensive. Comparative effectiveness research (CER), is a feasible alternative which can generate high-quality real-world evidence using real-world data, by comparing the impact of different clinical practices.

Aim: To conduct an international CER study, using a pragmatic clinical trial design, in conjunction with the existing infrastructure of the Canadian Neonatal Network to identify the optimal management of hypotension in very preterm neonates with suspected LOS.

Objective: To compare the relative effectiveness and safety of pharmacologically equivalent dosages of DA versus NE for primary pharmacotherapy for fluid-unresponsive hypotension in preterm infants born ≤ 32 weeks gestational age with suspected LOS.

Hypothesis: Primary treatment with NE will be associated with a lower mortality

Methods: This CER project will compare management approach at the unit-level allowing inclusion of all eligible patients admitted during the study period. 16 centers in Canada, 2 centers in Ireland, 1 center in each of Israel, Spain and the UK, and 6 centers in the United States have agreed to standardize their practice. All eligible patients deemed circulatory insufficient will receive fluid therapy (minimum 10-20 cc/kg). If hypotension remains unresolved:

Dopamine Units: start at 5mics/kg/min, increase every 16-30 minutes by 5 mics/kg/min to a maximum dose of 15 mics/kg/min or adequate response

Norepinephrine Units: start at 0.05 mics/kg/min, increase every 16-30 minutes by 0.05 mics/kg/min to maximum dose of 0.15/mics/kg/min or adequate response

Recruiting

Interested in participating?

Request Info

Key information

Age range

21 week–32 week

Sex eligibility

All sexes

Study type

Observational

Primary location

Foothill's Medical Centre, Calgary, Alberta, Canada

Loading trial locations.

About this study

In this study, we will use real world data (RWD; defined as data generated during routine clinical practice) collected by our national Canadian Neonatal Network (CNN), which will be further expanded for this project.

The CNN is a well-established patient registry that includes members from 31 hospitals and 17 universities across Canada. The Network maintains a standardized NICU database and provides a unique opportunity for researchers to participate in collaborative projects. We will use the framework of Hypotheses Evaluating Treatment Effectiveness (HETE) research a form of comparative effectiveness research (CER).

Patient registries are emerging as a new method for assessment of treatments under the framework of CER. We will evaluate treatment effectiveness of two routinely used primary therapies for hypotension management in very preterm neonates with suspected LOS after standardizing treatment strategies and with a priori hypothesis.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • ≤32 weeks gestational age and > 48 hours of life
  • Receiving primary vasopressor therapy with Dopamine or Norepinephrine in the context of suspected late-onset sepsis or necrotizing enterocolitis with systemic hypotension (defined as: culture positive or negative bloodstream infection)

Exclusion criteria

  • Known chromosomal or genetic anomalies
  • Receiving primary therapy with agents other than Dopamine or Norepinephrine

Treatment and study plan

Dopamine

Drug

Start at 5mics/kg/min, increase every 16-30 minutes by 5 mics/kg/min to a maximum dose of 15 mics/kg/min or adequate response.

norepinephrine

Drug

Start at 0.05 mics/kg/min, increase every 16-30 minutes by 0.05 mics/kg/min to maximum dose of 0.15/mics/kg/min or adequate response

Primary outcomes

  1. All cause in-hospital mortality

    Time frame: From illness onset to discharge (home or to another hospital) - assessed up to a maximum of 36 weeks after date of birth

    Death before discharge

Secondary outcomes

  1. Episode-related death

    Time frame: <14 days from illness onset

    Episode-related death (yes or no- binary variable)

  2. Treatment failure rate

    Time frame: 90 minutes after initial vasopressor initiation (or sooner if secondary dose added or primary agent replaced as per clinical discretion)

    Need for further dose escalation or use of additional agents (treatment failure = hypotension unresolved after reaching max dose (15mics/kg/min in Dopamine units and 0.15 mics/kg/min in Norepinephrine units)

  3. New diagnosis of severe neurological injury

    Time frame: From illness onset to discharge (home or to another hospital) - assessed up to a maximum of 36 weeks after date of birth

    Grade III or Grade IV intraventricular hemorrhage or periventricular leukomalacia (yes or no- binary variable)

  4. Bronchopulmonary dysplasia

    Time frame: Assessed at 36 weeks PMA

    Need for oxygen or positive pressure respiratory support at 36 weeks postmenstrual age (PMA) (yes or no- binary variable)

  5. Retinopathy of prematurity

    Time frame: From illness onset to discharge (home or to another hospital) - assessed up to a maximum of 36 weeks after date of birth

    Diagnosis of retinopathy of prematurity - assessed by clinical staff (yes or no - binary variable)

  6. Length of hospital stay

    Time frame: From admission date to discharge date - assessed up to a maximum of 36 weeks after date of birth

    Length of entire neonatal intensive care unit stay from admission to discharge

Study contacts

Contact information is provided by the study sponsor or research team.

Amish Jain, MBBS, MRCPCH, PhD

CONTACT

[email protected]

416-586-4800 ext. 5459

Laura Thomas, MSc

CONTACT

[email protected]

416-586-4800 ext. 172060

Sponsors and collaborators

Lead sponsor

Mount Sinai Hospital, Canada

Other

Collaborators

  • Assaf-Harofeh Medical Center
  • BC Women's Hospital & Health Centre
  • Banner University Medical Center
  • Children's Hospital at Montefiore
  • Children's Hospital of Eastern Ontario
  • Coombe Women and Infants University Hospital
  • Dayton Children's Hospital
  • Foothills Medical Centre
  • Golisano Children's Hospital
  • Health Sciences Centre, Winnipeg, Manitoba
  • Hospital Universitario La Paz
  • IWK Health Centre
  • Island Health, Victoria, BC
  • Jewish General Hospital
  • London Health Sciences Centre
  • McMaster Children's Hospital
  • Methodist Healthcare - Memphis
  • St. Boniface Hospital
  • St. Justine's Hospital
  • Stony Brook University
  • Sunnybrook Health Sciences Centre
  • The Hospital for Sick Children
  • University College Cork
  • Windsor Regional Hospital

Registry information

Official study title

Dopamine vs. Norepinephrine for Hypotension in Very Preterm Infants With Late-onset Sepsis: An International Comparative Effectiveness Research Project

Important dates

Study start
2023
Primary completion
2026
Study completion
2027
First posted
Apr 26, 2022
Registry last updated
Jul 8, 2025

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.

Published trials that share one or more normalized conditions with this study.