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

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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04081142
Enrollment
119
Registered
2019-09-09
Start date
2018-05-01
Completion date
2020-07-31
Last updated
2020-12-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

ARDS, Human, Hypoxemia, Respiratory Failure

Keywords

EIT, pulmonary perfusion

Brief 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

Detailed 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.

Interventions

None listed

Sponsors

Yun Long
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Lung regional perfusionHour 1Lung regional perfusion monitored by EIT with saline
oxygenationHour 1oxygenation(SpO2) measured by bedside monitor

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 14, 2026