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NCT04081142 Clinical Trial

Application of Indicator Based-electrical Impedance Tomography Method Assess Lung Regional Perfusion in ICU Patients

Respiratory Failure Clinical Trial

Official title:
Application of Indicator Based-EIT Method Assess Lung Regional Perfusion for Critically Ill Patients in ICU

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04081142
Other study ID # EIT-lung Perfusion in ICU
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 1, 2018
Est. completion date July 31, 2020

Study information
Verified date December 2020
Source Peking Union Medical College Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study is an observational study. Investigate the relationship of oxgenation and lung regional ventilation and perfusion assessed by the indicator based-EIT method in the critically ill patients in ICU

Description:

1. Written informed consent was obtained from all patients or next of kin before data were included in the study. 2. When the research team was available, adult patients within 1w, who were sequentially admitted to the Department of Critical Care Medicine and required central venous catheters for resuscitation were eligible for the study. 3. Information collected at enrollment included demographic characteristics such as age, sex, Acute Physiology and Chronic Health Evaluation II score (APCHEII); . The global hemodynamic, respiration condition and PaO2 were measured. At the same time, the lung regional ventilation and perfusion assessed by the indicator based-EIT method(injection 10%NaCL). 4. The 10%NaCL was injected by the central venous catheter.

Recruitment information / eligibility
Status Completed
Enrollment 119
Est. completion date July 31, 2020
Est. primary completion date July 31, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Time of admission ICU < 7days - Age (> 18 years old) - Have been placed central venous catheter based on clinical requirement Exclusion Criteria: .Chest skin injured and cannot be monitored by EIT. - Severe Hypernatremia - Pregnancy

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
China Peking Union Medical College Hospital, Chinese Academy of Medical Science Beijing Beijing

Sponsors (1)
Lead Sponsor Collaborator
Yun Long

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary Lung regional perfusion Lung regional perfusion monitored by EIT with saline Hour 1
Primary oxygenation oxygenation(SpO2) measured by bedside monitor Hour 1
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