MedDataX Logo

Respiratory Volume Measure Using ExSpiron 1Xi

NCT ID: NCT02998294

Last Updated: 2018-07-18

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

63 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-04-06

Study Completion Date

2017-02-15

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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.

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

Detection of Postoperative Respiratory Depression in High Risk Patients Utilizing Minute Ventilation Monitoring

NCT04017702

Respiratory Depression
COMPLETED

Evaluation of ExSpiron™ Measurements Derived Without Patient Specific Calibration

NCT02690298

Non-Invasive Respiratory Volume Monitoring
COMPLETED

Evaluation of Non-Invasive Respiratory Volume Monitor

NCT03039881

Monitoring for Low Minute Ventilation Post Surgery
COMPLETED

A New Tool for Extubation Readiness in Mechanically Ventilated Patients: Readiness for EXtubation Score

NCT07098611

Ventilator Weaning Respiration, Artificial Respiratory Failure +5 more
RECRUITING

The Use of ExPreS in the Weaning of Patients in Invasive Mechanical Ventilation

NCT05085457

Respiratory Insufficiency
COMPLETED NA

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

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.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

ICU(Intensive Care Unit) Patients Mechanical Ventilation After Surgery

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Respiratory monitoring group

Group Type EXPERIMENTAL

Respiratory Volume Monitor(RVM)

Intervention Type DEVICE

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

artificial respirator

Intervention Type DEVICE

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

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Respiratory Volume Monitor(RVM)

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

Intervention Type DEVICE

artificial respirator

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

Intervention Type DEVICE

Other Intervention Names

Discover alternative or legacy names that may be used to describe the listed interventions across different sources.

ExSpiron™ 1Xi

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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
Minimum Eligible Age

19 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Yonsei University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Department of Anesthesiology and Pain Medicine, Anesthesia and Pain Research Institute, Yonsei University College of Medicine

Seoul, , South Korea

Site Status

Countries

Review the countries where the study has at least one active or historical site.

South Korea

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

1-2016-0008

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Volume Responsiveness Before SBT Predicts the Outcome of Mechanical Ventilation Weaning in Critically Ill Patients
NCT01867853 COMPLETED
Effect of Lung Volume Recruitment Technique After Extubation
NCT05128552 COMPLETED NA
Oxygen Consumption (VO2), Effort, and Weaning in the Mechanically Ventilated Patient in the Intensive Care Unit (ICU)
NCT06391424 RECRUITING
Evaluation of the Therapeutic Usability of RESPIRA ADVANCED Device in Patients Under Invasive Mechanical Ventilation
NCT05174130 UNKNOWN NA
Assessments of Diaphragm-pleural Mechanics During the Weaning From Prolonged Mechanical Ventilation
NCT03842280 UNKNOWN
Comparison of Diaphragm Ultrasound and RSBI for Predicting Weaning Success in Mechanically Ventilated ICU Patients
NCT07120438 NOT_YET_RECRUITING
Expiratory Time Constant in Mechanically Ventilated Patients
NCT05827640 COMPLETED
Postoperative Respiratory and Activity Monitoring
NCT06239831 RECRUITING
New Automated System for Continuous Real-time Monitoring of Transpulmonary Pressure
NCT03945409 UNKNOWN
Improving Our Understanding of Respiratory Muscle Training to Facilitate Weaning From Mechanical Ventilation in the ICU
NCT04658498 RECRUITING NA
Monitoring Intercostal Muscles After Extubation
NCT02853201 COMPLETED
Detection of SpO2-oscillations of Low Ventilated Areas
NCT02022969 WITHDRAWN
Intubation and Extubation Over 48 Hours Mechanical Ventilation
NCT01123681 UNKNOWN
Determination of the Optimal Spontaneous Breathing Trial During Weaning of Mechanical Ventilation
NCT04222569 TERMINATED NA
Proportional Assist Ventilation Plus and Estimation of Respiratory Effort During the Transition to Spontaneous Ventilation
NCT06998927 ACTIVE_NOT_RECRUITING
Respiratory Mechanics Measurement of Ventilated Patients Through Low-frequency Oscillometry Technique
NCT06483529 RECRUITING NA
Deventilation Dyspnea in COPD Patients Using NIV
NCT03503123 COMPLETED
Predictive Analysis Software for Successful Weaning From Ventilator of Patients
NCT02915458 UNKNOWN
Respiratory Knowledge Portal Computer and Phone Application to Improve Quality of Mechanical Ventilation by Reducing the Number of Ventilator Associated Events, Injury Created by the Ventilator and Unsafe Setting of Alarms.
NCT06737432 RECRUITING NA
Comparative Study of Non-Invasive Mask Ventilation vs Cuirass Ventilation in Patients With Acute Respiratory Failure.
NCT00331656 UNKNOWN PHASE4
Specific Inspiratory Muscle Training (SIMT)in the Patients With Ventilatory Dependence
NCT00792441 UNKNOWN NA
Low-Intensity Mechanical Ventilation in the Operating Room: a Pilot Study
NCT07277244 NOT_YET_RECRUITING NA
Evaluation of Prolonged Apnea Supported by High Frequency Non-invasive Ventilation.
NCT02712190 UNKNOWN NA
A Study on the Assessment of Difficult Weaning in Patients With Acute Respiratory Failure Undergoing Mechanical Ventilation Based on Machine Learning EIT-pendelluft: A Multicenter Retrospective Study.
NCT06756204 ACTIVE_NOT_RECRUITING
Effects of Invasive Mechanical Ventilation on the Right Ventricular Function
NCT05710419 UNKNOWN