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Interobserver Variation in Applying a Radiographic Definition for Acute Respiratory Distress Syndrome (ARDS)

S

Society of Critical Care Medicine, China

Status

Completed

Conditions

Acute Respiratory Distress Syndrome

Treatments

Other: Training and education

Study type

Observational

Funder types

Other

Identifiers

NCT01704066
CCCCTG-2012-ARDS-01
2012BAI11B05 (Other Grant/Funding Number)

Details and patient eligibility

About

The original American-European Consensus Conference (AECC) definition of Acute Respiratory Distress Syndrome (ARDS) required bilateral infiltrates consistent with pulmonary edema on frontal chest X-ray (CXR), but there is poor inter-observer reliability in interpreting CXR using this definition among intensivists and radiologists.

As a result, the newly published Berlin definition of ARDS specified that the CXR criterion should include bilateral opacities consistent with pulmonary edema not fully explained by effusions, lobar/lung collapse, or nodules/masses on CXR.

In order to improve inter-observer agreement, the panel have also developed a set of CXRs judged as consistent, inconsistent, or equivocal for the diagnosis of ARDS.

The objective of this study is to investigate the impact of this training set on inter-observer reliability in applying the radiographic definition for ARDS.

Full description

The study is composed of 3 phases:

Phase 1: All participants will be required to independently interpret a set of 12 CXRs, as provided by the consensus panel. The possible radiographic interpretations include consistent, inconsistent, or equivocal for the diagnosis of ARDS.

Phase 2: Training materials adapted according to the recently published Berlin definition of ARDS, with its expanded rationale and interpretation of all 12 CXRs, will be sent to all participants.

Phase 3: The same set of 12 CXRs, in different order, will be sent to all participants for interpretation for the second time.

Enrollment

286 patients

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • intensivists working in the participating ICUs

Exclusion criteria

  • those who could not participate both questionnaire surveys
  • those who have read the reference with the training set of CXRs before the study
  • those who have already known the objective of the study

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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