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PEEP FOR LUNG RECRUITMENT IN PRETERM INFANTS-EIT STUDY

EFFECT OF VARYING LEVELS OF PEEP ON PRETERM LUNG RECRUITMENT USING ELECTRICAL IMPEDANCE TOMOGRAPHY- FEASIBILITY STUDY

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06705257
Acronym
[PEOPLE]
Enrollment
30
Registered
2024-11-26
Start date
2025-06-15
Completion date
2026-12-31
Last updated
2026-05-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Electrical Impedance Tomography (EIT), Lung Recruitment, Positive End Expiratory Pressure (PEEP), PreTerm Neonate

Keywords

positive end expiratory pressure, PRETERM, Electrical Impedance Tomography

Brief summary

Babies born early (under 32 weeks) are at risk of developing lung problems after birth. A major reason for this is that the lungs are not fully developed. Lungs of preterm babies will often collapse in between breathing due to lung immaturity. Applying gentle pressure, using nasal device through their nostril or through the breathing tube helps to prevent this lung collapse. This would help in air-oxygen going to lungs and also makes the babies breathing more comfortable. This gentle pressure is medically called as PEEP/CPAP and could be delivered by breathing machine (ventilator) and CPAP machine, collectively called as "continuous distending pressure (CDP)". Those babies breathing on their own and receiving inadequate CDP would need more breathing support by placing them on breathing machine (ventilator). The longer the baby receives breathing machine support, higher chance of lung injury . Preterm infants who are already on breathing machine, providing sub optimal PEEP/CPAP could also lead to lung damage. Providing optimal PEEP/CPAP could prevent these negative outcomes. Currently there is not enough evidence to suggest optimal PEEP/CPAP in preterm infants. Neonatal units all around the world uses PEEP/CPAP ranging from 4 to 10cm H20 based on their unit practice. Currently available investigations provide limited one time information (e.g. Chest X-ray) regarding whether baby is receiving optimal PEEP/CPAP. Electrical Impedance Tomography (EIT) is a new technology which could provide better information regarding the pressure delivered. Also, this device would provide continuous information as if the clinicians are doing continuous chest X-ray but without any radiation. In this study, the team will assess the effect of different levels of PEEP/CPAP (4 to 10cm H20) on prevention of lung collapse using EIT. This would be studied in premature infants who are on breathing machine support and CPAP machine support.

Interventions

DIAGNOSTIC_TESTStudying the effects of varying levels of PEEP using Electrical impedance tomography

Feasibility of using EIT, to study the effect of varying levels of PEEP/Continous distending pressure on lung recruitment as measured by changes in functional lung scores and silent spaces in preterm infants (\<32 weeks) who are on mechanical ventilation or receiving primary or post extubation CPAP support.

Sponsors

South Tees Hospitals NHS Foundation Trust
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Intervention model description

Single arm. All the recruited preterm infants will undergo increasing and decreasing levels of PEEP and the effect of EIT with various PEEP levels will be studied.

Eligibility

Sex/Gender
ALL
Age
22 Weeks to 32 Weeks
Healthy volunteers
No

Inclusion criteria

1. Gestational age \<32 weeks based on mother's last menstrual period or first trimester ultrasound dating. 2. Receiving either CPAP or mechanical ventilation respiratory support. 3. Informed written consent from one of the parents. 4. Within the first two weeks of life. Investigators pragmatically chose this period, as there could be considerable lung injury after the first two weeks of life, making it difficult to test our hypothesis. Also, this time period would allow parents to settle down with their stressful preterm delivery and investigators could approach anytime within the first two weeks of life.

Exclusion criteria

1. Major congenital malformations including congenital lung disease and congenital heart disease as ascertained by the medical team. 2. Infants diagnosed with pneumothorax i. 3. Receiving high frequency mechanical ventilation. 4. Infants with concerns of skin integrity.

Design outcomes

Primary

MeasureTime frameDescription
Changes in EIT parameterstotal study of 280 minutesChanges in End expiratory Lung Impedance scores
Changes in EIT280 minutesChanges in silence spaces with varying levels of CDP.

Secondary

MeasureTime frameDescription
Secondary outcomesTotal 280 minutes of study timeChanges in oxygen saturation (SpO2 in percentage) during the study period.
Secondary outcome measureTotal study time of 280 minutesChanges in carbon dioxide levels as measured by transcutaneous carbon dioxide levels (TCO2) in kilopascal.
Secondary outcomeTotal study time of 280 minutesChanges in fraction of inspiratory oxygen (Fio2) levels during the study.

Countries

United Kingdom

Contacts

CONTACTPrakash Kannan Loganathan, MD
pkannanloganathan@nhs.net+447481492632
CONTACTAmanda Forster
amanda.forster2@nhs.net+44 1642 854872
STUDY_DIRECTORJackie Mitchell

South Tees NHS foundation trust

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 7, 2026