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Effect of respiratory parameters of EIT titration on patients with moderate and severe ARDS

Effect of respiratory parameters of EIT titration on patients with moderate and severe ARDS

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300067928
Enrollment
Unknown
Registered
2023-01-31
Start date
2023-01-20
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

ARDS

Interventions

Test group:VT by EIT titration

Sponsors

Zhongda Hospital, Southeast University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: Age >=18 years old;Definite diagnosis of ARDS (Berlin definition);The course of the disease is not less than 7 days

Exclusion criteria

Exclusion criteria: Contraindications exist for EIT; Previous chronic respiratory disease (long-term home oxygen therapy for chronic respiratory disease such as pulmonary fibrosis or COPD); No informed consent was signed; Grade 3-4 cardiac insufficiency

Design outcomes

Primary

MeasureTime frame
respiratory system compliance;

Secondary

MeasureTime frame
Dead Space ratio;SI;overdistension monitored by EIT;collapse monitored by EIT;change in EELV;COV;RVD;RI index;

Countries

China

Contacts

Public ContactLing Liu

Zhongda Hospital, Southeast University

2324858754@qq.com+86 15901599659

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026