Respiratory Volume Measure Using ExSpiron 1Xi

Not Applicable

Completed

• Conditions: ICU(Intensive Care Unit) Patients; Mechanical Ventilation After Surgery
• Interventions: Device: Respiratory Volume Monitor(RVM); Device: artificial respirator

• Registration Number: NCT02998294
• Lead Sponsor: Yonsei University

Brief Summary

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.

Detailed Description

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.

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.

Study Timeline

• Study Start: 2016-04-06
• Study First Submitted: 2016-12-13
• Study First Submitted QC: 2016-12-15
• Study First Posted: 2016-12-20
• Primary Completion: 2017-02-15
• Study Completion: 2017-02-15
• Status Verified: 2018-07
• Last Update Submitted: 2018-07-15
• Last Update Posted: 2018-07-18

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 63

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.

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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

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Respiratory monitoring group	artificial respirator	-
Respiratory monitoring group	Respiratory Volume Monitor(RVM)	-

Primary Outcome Measures

Name	Time	Method
Respiratory volume measure using ExSpiron 1Xi	during 10-minute	During mechanical ventilator, we obtained respiratory parameter from ventilator and also we collected same parameter via RVM.

Trial Locations

Locations (1)

Department of Anesthesiology and Pain Medicine, Anesthesia and Pain Research Institute, Yonsei University College of Medicine; 🇰🇷 Seoul, Korea, Republic of