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
Procedure: weaning protocol
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Full eligibility criteria for NCT03027713
Ages eligible for Study
18 Years to 80 Years
Genders eligible for Study
Accepts Healthy Volunteers
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.
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.
All locations for NCT03027713
View full eligibility
Tris trial is registered with FDA with number: NCT03027713. The sponsor of the trial is Fundación para la Investigación del Hospital Clínico de Valencia and it is looking for 40 volunteers for the current phase.
Official trial title: Diaphragmatic Activity During a Postoperative Rapid Weaning Protocol With Neurally Adjusted Ventilatory Assist in Healthy Lung Patients, a Pilot Study.
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