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The Study of EIT-guided Ventilation Strategy on ARDS Patients

Chinese Academy of Medical Sciences & Peking Union Medical College logo

Chinese Academy of Medical Sciences & Peking Union Medical College

Status

Unknown

Conditions

Pulmonary Perfusion
ARDS

Treatments

Procedure: EIT-guided PEEP setting
Procedure: ARDS-net PEEP setting

Study type

Interventional

Funder types

Other

Identifiers

NCT04734340
EIT-RCT

Details and patient eligibility

About

This study is a clinical randomized controlled study.The objective of this study is to compare the prognosis of patients with ARDS between eit-v / q-oriented individualized ventilation strategy and traditional lung protection ventilation strategy, and to establish the demonstration application of eit-v / q-oriented ventilation strategy in ARDS

Enrollment

100 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. According to ARDS Berlin standard, ARDS, PaO2 / FiO2 < 200mmhg, peep > 5cmh2o;
  2. According to clinical judgment, lung recruitment therapy is needed due to hypoxemia;
  3. The subjects or their families signed informed consent.
  4. Admission to ICU was less than 72 hours;
  5. The estimated duration of mechanical ventilation was more than or equal to 48 hours;
  6. Age ≥ 18 years old and ≤ 80 years old;

Exclusion criteria

  1. The patients with heart implants could not be monitored by EIT;
  2. Patients or their families refused to participate in the study;
  3. Hypernatremia

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

100 participants in 2 patient groups, including a placebo group

EIT-guided group
Experimental group
Description:
Treatment based on EIT
Treatment:
Procedure: EIT-guided PEEP setting
Control group
Placebo Comparator group
Description:
Treatment based on ARDS-net Peep setting
Treatment:
Procedure: ARDS-net PEEP setting

Trial contacts and locations

1

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Central trial contact

Yun Long; Siyi Yuan

Data sourced from clinicaltrials.gov

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