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NCT05812365

Best End-Expiratory and Driving-pressure for Individualized Flow Controlled Ventilation in Patients With COPD

Completed Last updated 25 July 2024
What this trial tests

trial in COPD in 10 participants. Completed in 24 July 2024.

Timeline
1 July 2024
Primary endpoint
24 July 2024
24 July 2024

Quick facts

Lead sponsorUniversitätsklinikum Hamburg-Eppendorf
StatusCompleted
Study typeOBSERVATIONAL
Enrollment10
Start date1 July 2024
Primary completion24 July 2024
Estimated completion24 July 2024
Sites1 location across Germany

Conditions studied

Sponsor

Universitätsklinikum Hamburg-Eppendorf — full company profile →

Who can join

18 and older, any sex, with COPD or Ventilator Lung. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Patients with chronic obstructive pulmonary disease (COPD) have a significantly increased risk of postoperative pulmonary complications (PPC). Protective ventilation of the lungs could reduce the rate of PPC in patients with COPD. It has been suggested that flow controlled ventilation (FCV) may be less invasive and more protective to the lungs than conventional ventilation in patients with COPD. The primary aim of this study is to determine a optimal individual ventilation setting for FCV in ten participants with COPD.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for COPD

Currently open trials in the same condition.

Other Universitätsklinikum Hamburg-Eppendorf trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05812365.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing