Respiratory Volume Measure Using ExSpiron 1Xi

Yonsei University

Status

Completed

Conditions

Mechanical Ventilation After Surgery

ICU(Intensive Care Unit) Patients

Treatments

Device: artificial respirator

Device: Respiratory Volume Monitor(RVM)

Study type

Interventional

Funder types

Other

Identifiers

NCT02998294

1-2016-0008

Details and patient eligibility

About

The purpose of this study was to determine the accuracy of one-time respiratory volume measured by RVM(Respiratory Volume Monitor) compared to the one-time respiratory volume measured by mechanical ventilation in post-operative ICU patients.

Full description

In addition, the investigators investigated the decrease in respiratory volume in opioid infusion after ventilator weaning in this patient, and to measure the one-time respiratory volume change by RVM during deep breathing induction using Inspirometry exercise.

Enrollment

63 patients

Sex

All

Ages

19+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

An adult patients ( ≥ age 19)
patients who receive mechanical ventilation in the ICU of the Severance Hospital after surgery and plans to wean the mechanical ventilation within 3 days.

Exclusion criteria

severe respiratory illness patients (pneumothorax, chest tube intubation status, severe restrictive respiratory disease, unilateral lung ventilation, lung transplantation status, chronic restrictive respiratory disease, hydrothorax, diaphragmatic movement disorder)
If the candidate can not understand and carry out the experiment contents and process