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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03763890
Other study ID # 20181129PEEP
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date September 1, 2018
Est. completion date December 30, 2023

Study information

Verified date July 2022
Source Southeast University, China
Contact ling Liu, Phd
Phone 13851435472
Email liulingdoctor@126.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study try to use EIT ( Electronic impedance tomography ) to evaluate the alveolar heterogeneity and use trans-pulmonary pressure and stain to evaluate the lung injury . The study use these methods to figure out how PEEP impact the alveolar heterogeneity and VILI.


Description:

ARDS(Acute respiratory distress syndrome )is common in patients suffering Sepsis, trauma, burning and other sever condition and characterized by diffuse alveolar damage and alveolar heterogeneity.ARDS patient need MV(mechanical ventilation )to maintain oxygenation and need unique MV tragedy to avoid VILI(Ventilator induced Lung injury ).PEEP(post-end-expiratory pressure) is crucial to maintain oxygenation and avoid VILI according to researches. But there are also some other research different voice. This study try to use EIT ( Electronic impedance tomography ) to evaluate the alveolar heterogeneity and use trans-pulmonary pressure and stain to evaluate the lung injury . The study use these methods to figure out how PEEP impact the alveolar heterogeneity and VILI.


Recruitment information / eligibility

Status Recruiting
Enrollment 40
Est. completion date December 30, 2023
Est. primary completion date December 30, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: 1. Age=18 or<80; 2. Moderate or sever ARDS in 2012 <Berlin definition>; 3. Applied mechanical ventilation; 4. Consent signed. Exclusion Criteria: 1. Asthma or COPD; 2. Cardiogenic edema; 3. Sever neutropenia(<500/mm3); 4. Hemodynamic astatic: DOPA or Dobutamine >15 µg/kg/ min; NE > 15ug /min; 5. GCS coma score =12; 6. Thoracic injury or surgery patients contradict EIT ; 7. Refuse to join in trail; 8. Included in other clinical trail?

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Post-end-Expiratory pressure
Titrate the PEEP from 24 cmH2O to 6 cmH2O, 2 cmH2O/step and record EIT, trans-pulmonary pressure, hemodynamic parameter and Blood-gas analysis.

Locations

Country Name City State
China Nanjing Zhong-Da Hospital Nanjing Jiangsu

Sponsors (1)

Lead Sponsor Collaborator
Southeast University, China

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary alveolar hyper-distention; alveolar collapse;alveolar opening and closing; The study use Pulmo Vista 500 device (Drager co.),is intended to perform thoracic bioimpedance measurements by applying the technique of electrical impedance tomography (EIT)to evaluate alveolar hyper-distention(%of the lung volume); alveolar collapse(% of the lung volume);alveolar opening and closing(% of the lung volume). September,1,2018-December 30, 2020
Primary Trans-pulmonary pressure The researchers place tube in the esophagus and connect it to transmitter to measure esophageal pressure (mmHg)and calculate trans-pulmonary pressure(mmHg) to evaluate stress September,1,2018-December 30, 2020
Primary EELV The research use nitrogen wash out to measure EELV(end-expiratory lung volume, ml) to calculate dynamic strain and evaluate the strain September,1,2018-December 30, 2020
Primary peak pressure The researchers use ventilator to measure peak pressure(cmH2O) in patients with mechanical ventilation and without spontaneous breathing.. September,1,2018-December 30, 2020
Primary plateau pressure The researchers use ventilator to do inspiration pause to measure plateau pressure(cmH2O) in patients with mechanical ventilation and without spontaneous breathing. September,1,2018-December 30, 2020
Primary tidal volume The researchers use ventilator to measure tidal volume(ml) in patients with mechanical ventilation and without spontaneous breathing.. September,1,2018-December 30, 2020
Primary respiratory rate The researchers record the set respiratory rate(bpm) in patients with mechanical ventilation. September,1,2018-December 30, 2020
Primary flow The researchers record the set Flow (L/min) in patients with mechanical ventilation. September,1,2018-December 30, 2020
Primary FiO2 The researchers record the set FiO2 ( fraction of inspiratory oxygen, %) in patients with mechanical ventilation. September,1,2018-December 30, 2020
Primary PaO2 The researchers use blood gas analysis to measure PaO2( arterial oxygen pressure,mmHg) September,1,2018-December 30, 2020
Primary PaCO2 The researchers use blood gas analysis to measure PaCO2( arterial carbon dioxide pressure,mmHg) . September,1,2018-December 30, 2020
Secondary SBP Recording SBP(systolic pressure, mmHg),which is always continuously monitored with invasive pressure monitor. September,1,2018-December 30, 2020
Secondary DBP Recording DBP(Diastolic pressure, mmHg),which is always continuously monitored with invasive pressure monitor. September,1,2018-December 30, 2020
Secondary CVP Recording CVP(central venous Pressure),which is always discontinuously monitored with jugular pressure monitor mmHg). September,1,2018-December 30, 2020
Secondary vasopressor Recording clinical vasopressor usage including Norepinephrine( µg/Kg/min;)Epinephrine(µg/Kg/min) Dobutamine ( µg/Kg/min) September,1,2018-December 30, 2020
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