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Optimization of PEEP for Alveolar Recruitment in ARDS (OPERA)

H

Hopital of Melun

Status

Completed

Conditions

ARDS

Treatments

Device: esophageal pressure mesurement

Study type

Observational

Funder types

Other

Identifiers

NCT01949272
OPERA (Other Identifier)

Details and patient eligibility

About

Actual setting of PEEP in ARDS is based on tables linked to FiO2, or respiratory system plateau pressure (e.g EXPRESS Study) or set regarding esophageal pressure mesurement and transpulmonary pressure calculation. Opera study should confirm if a setting approach based on esophageal pressure is helpfull for any ARDS patient in ICU without deleterious side-effect.

Enrollment

22 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • ARDS Stades 2 and 3 with invasive ventilation (EXPRESS settings) within 3 to 12 hours

Exclusion criteria

  • less 18 years, pregnancy, intracardiac shunt, esophageal catheter cons-indicated

Trial design

22 participants in 1 patient group

ARDS
Description:
ARDS patients achieving stades II and III of Berlin 2011 Classification
Treatment:
Device: esophageal pressure mesurement

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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