Clinical Validation of Continuous and Non-invasive Monitoring of Effective Pulmonary Volume.

NCT04045262 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 85

Last updated 2022-10-12

No results posted yet for this study

Summary

The aim of this study is to evaluate/validate a new non-invasive method to continuously monitor effective lung volume in critically ill patients.

Conditions

  • Critical Illness

Sponsors & Collaborators

  • Fernando Suarez Sipmann

    lead OTHER

Principal Investigators

  • Fernando Suarez Sipmann, MD PhD · Fundación de Investigación Biomédica - Hospital Universitario de La Princesa

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-06-04
Primary Completion
2022-03-30
Completion
2022-03-30

Countries

  • Spain

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 NCT04045262 on ClinicalTrials.gov