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COMPLETEDNA

PNEUMACRIT Device for Neonatal Cardio Respiratory Monitoring

Preterm Neonate/ Neonatal Embedded Universal Microelectronic Wearable Acquisition for Cardio Respiratory Intensive Therapy. Clinical Assessment of Device Usability and Reliability

NCT06171867•University of Oulu

View on ClinicalTrials.gov

Summary

The usability of a new PNEUMACRIT system is studied in clinical environment in this feasibility study.

Detailed Description

Electrical impedance tomography is a noninvasive monitoring tool for neonatal lung aeration and breathing. This feasibility study will assess the usability of a new PNEUMACRIT electrode belt in clinical environment.

Eligibility

Age

0 - 0 years

Sex

ALL

Healthy Volunteers

Inclusion Criteria

•Inpatient at Oulu University Hospital PICU or NICU
•Gestational age at birth over 32 weeks
•Weight 2000-5000g
•Postnatal age \> 12 hours
•Written informed consent from the parents of legal representative
•Non-invasive monitoring of oxygen saturation and ECG

Exclusion Criteria

•Postmenstrual age \< 32 weeks
•Weight at time of the study \< 2000g or \> 5000g
•Chest skin lesion preventing safe use of the electrode belt
•Recent chest surgery within the past 7 days (e.g. thoracotomy)

Locations (1)

Oulu University Hospital

Oulu, Finland

Key Dates

Start Date

November 24, 2023

Primary Completion Date

February 25, 2024

Completion Date

February 25, 2024

Last Updated

February 28, 2024

Enrollment

ACTUAL participants

Conditions

Neonatal Respiratory Distress

Interventions

PNEUMACRIT

DEVICE

To Investigate the Effect of Pulmonary Surfactant With Different Inspired Oxygen Concentrations on the Clinical Outcomes of Very Preterm Infants Under Non-invasive Assisted Ventilation

NCT07235345

Neonatal Respiratory Distress Syndrome

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NOT_YET_RECRUITING

Lung Ultrasound in Neonatal Intensive Care Units

NCT06372951

Neonatal Respiratory Distress

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COMPLETEDNA

Effects of Kinesiotaping on Respiratory Muscles in Very Preterm Infants

Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: February 28, 2024Data synced to Clareo: March 29, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

View ClinicalTrials.gov Terms and Conditions

PNEUMACRIT Device for Neonatal Cardio Respiratory Monitoring

Inclusion Criteria

Exclusion Criteria

To Investigate the Effect of Pulmonary Surfactant With Different Inspired Oxygen Concentrations on the Clinical Outcomes of Very Preterm Infants Under Non-invasive Assisted Ventilation

Lung Ultrasound in Neonatal Intensive Care Units

Effects of Kinesiotaping on Respiratory Muscles in Very Preterm Infants

Aerosolized Infasurf Treatment Protocol: Aerosolized Infasurf for Spontaneously Breathing Patients With Early RDS (AERO-03)

Breastfeeding Infants Receiving Respiratory Support Trial

The Use of Maternal Serum Unconjugated Estriol for Monitoring the Prevention of Neonatal Respiratory Distress Syndrome