Weaning From Mechanical Ventilation Guide by Assessment of Lung Tidal Distribution With EIT

NCT ID: NCT03118804

Last Updated: 2022-11-30

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

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Recruitment Status

COMPLETED

Total Enrollment

55 participants

Study Classification

OBSERVATIONAL

Study Start Date

2016-10-18

Study Completion Date

2018-12-31

Brief Summary

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To evaluate whether EELI, RVD, GI were good predictor for weaning from mechanical ventilation

Detailed Description

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53 patients who ready to wean from mechanical ventilation were included in this study. The changes of lung tidal distribution during SBT with mechanical ventilation by EIT were recorded. Whether EELI, RVD, GI were good predictor for weaning from mechanical ventilation?

Conditions

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Mechanical Ventilation

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Weaning Guide by EIT

Weaning From Mechanical Ventilation Guide by Assessment of Lung Tidal Distribution With EIT

Assessment of Lung Tidal Distribution With EIT

Intervention Type DIAGNOSTIC_TEST

Changes of lung tidal distribution during SBT with mechanical ventilation were recorded by EIT can be used to predict weaning success or failure

Interventions

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Assessment of Lung Tidal Distribution With EIT

Changes of lung tidal distribution during SBT with mechanical ventilation were recorded by EIT can be used to predict weaning success or failure

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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Inclusion Criteria

1. Intubated patients age between 18 years old and 80 years old
2. Duration of controlled mechanical ventilation≥ 24 h
3. Patients ready to wean from mechanical ventilation
4. Informed consent

Exclusion Criteria

1. Pregnant women
2. Patients with malignant tumor
3. High paraplegia, neuromuscular lesions
4. Thoracic deformity, diaphragmatic hernia
5. Patients with ECMO
6. Patient participated in another interventional trial before enrollment
Minimum Eligible Age

18 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Southeast University, China

OTHER

Sponsor Role lead

Responsible Party

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Songqiao Liu

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Liu Songqiao, PHD

Role: PRINCIPAL_INVESTIGATOR

Southeast University

Locations

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Zhongda Hospital

Nanjing, Jiangsu, China

Site Status

Countries

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China

Other Identifiers

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2016ZDSYLL064-Y01

Identifier Type: -

Identifier Source: org_study_id

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