Viewing Study NCT06421506



Ignite Creation Date: 2024-06-16 @ 11:48 AM
Last Modification Date: 2024-10-26 @ 3:30 PM
Study NCT ID: NCT06421506
Status: NOT_YET_RECRUITING
Last Update Posted: 2024-05-22
First Post: 2024-05-09

Brief Title: Less Invasive Surfactant Administration in Late Preterm or Early Term Born Infants
Sponsor: Kings College Hospital NHS Trust
Organization: Kings College Hospital NHS Trust

Study Overview

Official Title: Does Less Invasive Surfactant Administration LISA During High-flow Nasal Cannula Oxygen Treatment Reduces the Need for Invasive Ventilation in Late Preterm and Term Born Infants With Respiratory Distress
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-05
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The aim of this study is to see if giving less invasive surfactant administration LISA during high-flow nasal cannula HFNC oxygen treatment reduces the need for invasive ventilation in babies with breathing problems born 2-6 weeks early

Less invasive surfactant administration is where surfactant a naturally produced substance which helps open up the tiny air sacs in the lungs making it easier for babies to breathe is given into the lungs by putting a small tube into the windpipe through the mouth whilst the baby is awake The surfactant is given slowly and breathed in

High flow nasal cannula is a form of non-invasive support where a machine delivers warmed moist oxygen and air through short tubes in the nose

The investigators will be assessing whether a lower percentage of neonates need invasive ventilation within 72 hrs from birth when they have had LISA during HFNC treatment compared to when they dont receive this treatment

The investigators will also be looking at the length of neonatal unit stay and the cost of the stay The investigators will also be measuring the lung function of the babies before and after they receive LISA
Detailed Description: This study is looking at babies born 2- 6 weeks early who have breathing problems soon after birth Some babies need to go onto a breathing machine ventilator or require non-invasive breathing support Either a machine delivers warmed moist oxygen air through short tubes in the nose humidified high flow nasal cannula HHFNC or a machine delivers oxygen and air via a small mask which fits over the nose continuous positive airway pressure CPAP Mechanical ventilation via a ventilator although life-saving can cause problems such as infection and lung injury and therefore whenever possible babys breathing is supported with non-invasive methods The use of CPAP in more mature babies may also cause discomfort or lung collapse whereas use of HHFNC may avoid those problems The lungs of healthy full-term babies naturally produce a substance called surfactant that helps open up the tiny air sacs in the lungs and makes it easier for them to breathe Babies born early or those with problems at birth do not have enough of their own surfactant or it does not work properly causing difficulty in taking in oxygen A natural animal-derived surfactant medication can be given into the lungs using a small tube put into the windpipe through the mouth This is done routinely in ventilated babies born prematurely More recently a technique called Less invasive surfactant administration LISA has been developed that allows us to give surfactant to babies who are receiving non-invasive breathing support ie HHFNC and thus avoiding the complications related to mechanical ventilation A small tube is passed into the windpipe whilst the baby is awake and breathing supported on HHFNC or CPAP and the surfactant is slowly given and breathed into the lungs At the moment there have been no research studies assessing the use of LISA in more mature infants receiving HHFNC as non-invasive respiratory support

In this study the investigators want to determine if in babies born between 34 and 386 weeks gestation who have breathing problems and receive HHFNC oxygen treatment with LISA within 24 hours of birth will reduce the need for mechanical ventilation The investigators will also be looking a the length on neonatal unit stay and the cost of the stay Lung function of the babies before and after they receive LISA will be measured

There will be no change in the management of babies taking part in the study Use of HHFNC administration of LISA and respiratory monitoring is all part of routine practice The investigators are asking for consent to analyse the routine monitoring that will be undertaken before during and after the surfactant administration and follow up on the outcome of the baby after they have had the LISA procedure

Surfactant is routinely used in babies and there are no extra risks from taking part in this study HHFNC is routinely used to support babies of this gestational age who require respiratory support There are no known or expected risks from using HHFNC with LISA but as of yet there have been no studies using this combination

Giving surfactant may help to avoid mechanical ventilation and its side effects but this has not been studied before in these gestational ages hence the need for this study Theoretically giving surfactant with HHFNC should aid even distribution of surfactant throughout the lungs whilst protecting the lungs from potential damage caused by other forms of non-invasive support such as CPAP but again there is not yet evidence supporting this

The study will be running at Kings College Hospital on the Neonatal Intensive Care Unit at the Denmark hill site and at the Local Neonatal Unit at the Princess Royal Hospital site The study has received ethical approval and is due to commence imminently May 2024 The study is aiming to recruit 245 patients which is estimated to take 2yrs and 4 months

The study is funded by Chiesi Limited The chief investigator for the study is Theodore Dassios theodoredassioskclacuk

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None