PNEUMACRIT Device for Neonatal Cardio Respiratory Monitoring

NCT06171867 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2024-02-28

No results posted yet for this study

Summary

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

Conditions

  • Neonatal Respiratory Distress

Interventions

DEVICE

PNEUMACRIT

Monitoring of breathing

Sponsors & Collaborators

  • Middlesex University

    collaborator OTHER
  • University of Oulu

    lead OTHER

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
12 Hours
Max Age
6 Months
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-11-24
Primary Completion
2024-02-25
Completion
2024-02-25

Countries

  • Finland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06171867 on ClinicalTrials.gov