Skip to main content
Clinical Trials/NCT03027713
NCT03027713
Completed
Not Applicable

Diaphragmatic Activity During a Postoperative Rapid Weaning Protocol With Neurally Adjusted Ventilatory Assist in Healthy Lung Patients, a Pilot Study.

Fundación para la Investigación del Hospital Clínico de Valencia0 sites40 target enrollmentJune 2009

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Postoperative Patients
Sponsor
Fundación para la Investigación del Hospital Clínico de Valencia
Enrollment
40
Primary Endpoint
Diaphragmatic electromyographic activity description
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The purpose of this study is to describe the diaphragm electromyographic activity (Edi) in healthy lung patients due to obtain a reference to guide the weaning in those patients

Detailed Description

We obtained the Edi recording data at each NAVA level during the weaning in NAVA group, and we compared the respiratory parameters between the PSV and NAVA groups

Registry
clinicaltrials.gov
Start Date
June 2009
End Date
June 2013
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Fundación para la Investigación del Hospital Clínico de Valencia
Responsible Party
Principal Investigator
Principal Investigator

F Javier Belda

Prof. Dr.

Fundación para la Investigación del Hospital Clínico de Valencia

Eligibility Criteria

Inclusion Criteria

  • Patients who were scheduled for elective major surgery in which admission to the CCU (critical care unit) for postoperative care and short-term mechanical ventilation with rapid weaning were anticipated.

Exclusion Criteria

  • Preoperative altered central nervous system, neuromuscular or lung disease and ASA (american society of anesthesiologists) classification group IV or NYHA (New York heart association) class IV in the case of cardiac patients. At the CCU, before randomisation, we also excluded patients requiring reoperation, and those who exhibited significant postsurgical bleeding, the development of myocardial infarction, and hemodynamic instability.

Outcomes

Primary Outcomes

Diaphragmatic electromyographic activity description

Time Frame: 1 hour

Similar Trials