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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03241654
Other study ID # KY-2017-001
Secondary ID
Status Completed
Phase N/A
First received August 3, 2017
Last updated February 9, 2018
Start date May 1, 2017
Est. completion date February 1, 2018

Study information

Verified date August 2017
Source Capital Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

In mechanically ventilated patients during supine position, alveolar collapse usually distributes in dependent lung region.Decrease of flow trigger sensitivity might improve homogeneous of tidal volume distribution.


Description:

In mechanically ventilated patients during supine position, alveolar collapse usually distributes in dependent lung region. High positive end expiratory pressure (PEEP) has been applied to improve the homogeneous distribution of ventilation by increasing the end expiratory lung ventilation (EELV) and alveolar recruitment. However, for patients who increasing PEEP in some extent still existed poor aeration in the dependent region, further elevating PEEP seems to be unreasonable that perhaps lead to overdistension. Decreasing trigger sensitivity might further evoke inspiratory efforts to improve the ventilation for this type of patients.The Electrical impedance tomography (EIT) was applied in monitoring the regional ventilation distribution at the bedside.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date February 1, 2018
Est. primary completion date August 20, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

1. The post operative patients who received pressure support ventilation;

2. After the clinical PEEP was evaluated 5cmH2O, the tidal volume distribution still existed heterogeneity.

Exclusion Criteria:

1. Under 18 years;

2. History of diaphragm dysfunction and surgery;

3. Central respiratory drive dysfunction;

4. history of esophageal, gastric or lung surgery;

5. The contraindication of using EIT (pacemaker, defibrillator, and implantable pumps).

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
flow trigger
The flow trigger will be adjust during the pressure assist ventilation.

Locations

Country Name City State
China Jian-Xin Zhou Beijing Beijing

Sponsors (1)

Lead Sponsor Collaborator
Capital Medical University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary The homogeneity of distribution of tidal volume EIT was used to monitoring the homogeneity of distribution of tidal volume that was divided into two contiguous regions of interest (ROI) equally, the dependent and non-dependent area. The ratio of relative distribution of tidal ventilation of two ROI was calculated. within 20 minutes after changing flow trigger
Secondary Changes in global and regional EELV The change of EELV was measured after changing flow trigger based on the baseline level. within 20 minutes after changing flow trigger
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