Current Studies

Introduction

PLATIPUS will host domains in pregnancy and early life (the ‘neonatal’ period).

Pregnancy Domains will assess therapies in pregnant women and people at risk of preterm birth. If you are pregnant and at risk of having your baby early, find out more about currently active Pregnancy Domains below.

Neonatal Domains will assess therapies for babies born preterm. If you are a parent or caregiver of a preterm baby, find out more about currently active Neonatal Domains below.

Learn more by watching this short informational video.
Pregnancy Domains
IN DEVELOPMENT
active study
COMPLETED

PROMOAT

What is the optimal antibiotic regimen for women with premature, prelabour rupture of membranes (PPROM)?

Objective

To determine which antibiotic regimen given to pregnant women and people with preterm prelabour rupture of membranes (PPROM) is best at improving health outcomes for preterm infants.

Who will be eligible?

Pregnant women and people with preterm, prelabour rupture of membranes (PPROM) who meet the eligibility criteria and are receiving care at a hospital taking part in this trial.

Why is this important?

Preterm prelabour rupture of membranes (PPROM) is when a pregnant woman or person’s waters break early. Approximately 30-40% of women who go on to have a preterm birth experience PPROM. PPROM can lead to infections and other complications in mother and baby.

Antibiotics are routinely given to pregnant women and people who experience PPROM to reduce the risk of infection.

Why are we doing this study?

The antibiotics given after PPROM vary in Australia, Aotearoa New Zealand and worldwide. Evidence for some of these antibiotics is now quite old, and there is potential in other antibiotics that are already being used for this purpose.

PROMOAT will assess three common antibiotic regimens given after PPROM in Australia and Aotearoa New Zealand, to reduce uncertainty and understand which antibiotic is best in reducing the risk of infection in mother and baby.

Funder: NHMRC and MRFF

Ethics Reference: [Pending]

Trial Registration: [Pending]

Domain-Specific
Working Group

Assoc. Prof. Clare Whitehead

Chair, Maternal and Fetal Medicine Specialist

Prof. Katie Groom

PLATIPUS Lead (NZ); Maternal Fetal Subspecialist

Dr Lisa Dawes

Maternal Fetal Subspecialist (Trainee)

Prof. Joshua Vogel

Perinatal Epidemiologist

Prof. John Newnham

Professor, Obstetrics

Prof. Michelle Giles

Professor, Infectious Disease (Adults)

Prof. Steven Tong

Professor, Infectious Disease (Adults)

Dr Lesley Voss

Infectious Disease (Paediatrics)

Prof. Michael Stark

Neonatologist

Prof. Brett Manley

Professor, Neonatology

Dr Matthew Payne

Perinatal molecular microbiologist

Prof. Katherine Lee

Biostatistician

Dr Robert Mahar

Biostatistician

Ms Marnie Cochrane

Lived Experience Consultant

Dr Esther Woolston

Lived Experience Consultant

Assoc. Prof. Clare Whitehead

Chair, Maternal and Fetal Medicine Specialist

Prof. Katie Groom

PLATIPUS Lead (NZ); Maternal Fetal Subspecialist


Dr Lisa Dawes

Maternal Fetal Subspecialist (Trainee)

Prof. John Newnham

Professor, Obstetrics

Prof. Michelle Giles

Professor, Infectious Disease (Adults)

Prof. Steven Tong

Professor, Infectious Disease (Adults)

Dr Lesley Voss

Infectious Disease (Paediatrics)

Prof. Brett Manley

Professor, Neonatology

Dr Matthew Payne

Perinatal molecular microbiologist

Prof. Katherine Lee

Biostatistician

Dr Robert Mahar

Biostatistician

Ms Marnie Cochrane

Lived Experience Consultant

Dr Esther Woolston

Lived Experience Consultant

Neonatal Domains
IN DEVELOPMENT
COMPLETED
active study

BabyCCINO

Comparing the different doses and regimens of caffeine given to very preterm infants with apnoea of prematurity (breathing problems)

Objective

To determine the optimal dose of caffeine citrate for very preterm infants experiencing apnoea of prematurity (breathing problems).

Who will be eligible?

Very preterm infants (babies born less than 32 weeks gestation) who meet the eligibility criteria and are receiving care at a hospital taking part in this trial.

Why is this important?

Apnoea of prematurity is when a baby born preterm stops breathing intermittently. It is common in preterm babies and occurs in almost all babies born at less than 28 weeks gestation.

Caffeine is routinely given to preterm babies who experience apnoea of prematurity. Caffeine has been shown to reduce both the number of times a baby stops breathing, and the number of babies who need additional help to breathe. This is important as it may also help to reduce the risk of other complications after birth and in the future.

Why are we doing this study?

The optimal dose of caffeine is unknown, and caffeine dosing practices vary in Australia, Aotearoa New Zealand and worldwide.

BabyCCINO will assess three common caffeine doses and dosing regimens that are given to babies born preterm in Australia and Aotearoa New Zealand, to reduce uncertainty and understand which dose is best for babies who experience apnoea of prematurity.

Funder: NHMRC and MRFF

Ethics Reference: [Pending]

Trial Registration: [Pending]

Lead Investigators: Professor Brett Manley and Associate Professor Chris McKinlay

Domain-Specific
Working Group

Prof. Brett Manley

Chair, Professor, Neonatology

Assoc. Prof. Chris McKinlay

Neonatal Lead (NZ)

Dr Kate Hodgson

Neonatologist

Assoc. Prof. Clare Whitehead

Maternal and Fetal Medicine Specialist

Prof. Peter Davis

Professor, Neonatology

Assoc. Prof. Jane Alsweiler
Assoc. Prof. Neonatology

Dr. Elizabeth Baker

Neonatologist

Dr. Tugba Alarcon-Martinez

Neonatology trainee

Assoc. Prof. Michael Stark
Neonatologist

Prof. Adrienne Gordon

Neonatologist

Dr. Elizabeth Oliphant

Lecturer, Pharmacy


Prof. Katherine Lee
Biostatistician


Dr Robert Mahar

Biostatistician

Ms. Amanda Sluiter

Lived Experience Consultant

Ms. Jessica Berry
Lived Experience Consultant

Get Involved
If you are eligible for one or more of the domains being run on PLATIPUS at your hospital, a member of the hospital research team will contact you to discuss PLATIPUS and invite you to participate.
Learn More