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Prevalence of Prone Positioning Use in ARDS Patients | Clinical Trials | Clareo Health

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Prevalence of Prone Positioning Use in ARDS Patients

Prospective Study on the Prevalence on the Use of Prone Positioning in ARDS Patients

NCT02842788•Hospices Civils de Lyon

Summary

Prone positioning has been shown to improve survival in patients with acute respiratory distress syndrome (ARDS). However, a recent large observational study found that prone positioning was used in only 7% of all ARDS patients, and 16% in the severe category. However, this study did not focus on the prone position per se. In present study, the investigators would like to explore the rate of use of prone positioning in ARDS patients and the reasons why this treatment was not applied. The present study is one-day prevalence study repeated four times over one year. The hypothesis is that the rate of use of prone position is greater than 50% in the severe ARDS category.

Eligibility

Age

18 - No limit years

Sex

ALL

Healthy Volunteers

Inclusion Criteria

•1.ARDS criteria (Berlin definition) fulfilled the day of the study, whatever the ARDS stage. The onset of ARDS could have been established at any time between ICU admission and study day but ARDS criteria must be still present the day of the study. The ARDS criteria are listed below
•* Within 1 week of a known clinical insult or new or worsening respiratory symptoms
•* Bilateral opacities-not fully explained by effusions, lobar/lung collapse, or nodules
•* Respiratory failure not fully explained by cardiac failure or fluid overload. Need objective assessment (eg, echocardiography) to exclude hydrostatic edema if no risk factor present
•2.PaO2/FIO2 ≤ 300 with PEEP ≥ 5 cmH2O
•3.Age ≥ 18 years
•4.Intubated or tracheotomized and mechanically ventilated

Exclusion Criteria

•Patient non intubated the day of the study
•No criteria for ARDS the day of the study even if these criteria were present between ICU admission and day of the study

Locations (1)

Réanimation médicale, Hôpital de la Croix Rousse, CHU de Lyon, France

Lyon, France

Key Dates

Start Date

April 1, 2016

Primary Completion Date

January 1, 2017

Completion Date

January 1, 2017

Last Updated

March 12, 2018

Enrollment

736

ACTUAL participants

Conditions

Acute Respiratory Distress Syndrome (ARDS)

Interventions

Prone positioning

PROCEDURE

Turning Ratios Into Prognosis: Neutrophil-to-Lymphocyte and Platelet-to-Lymphocyte Ratios as Powerful Predictors of ARDS in Pediatric Burn Patients: A Prospective Evaluation

NCT07414056

Acute Respiratory Distress Syndrome (ARDS)

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RECRUITINGPHASE2

JUST BREATHE, Breathing Life Into Innovative Therapies for ARDS- Cohort B: Paridiprubart

NCT06701669

Acute Respiratory Distress Syndrome (ARDS)ARDS+2 more

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: March 12, 2018Data synced to Clareo: March 29, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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Prevalence of Prone Positioning Use in ARDS Patients

Inclusion Criteria

Exclusion Criteria

Turning Ratios Into Prognosis: Neutrophil-to-Lymphocyte and Platelet-to-Lymphocyte Ratios as Powerful Predictors of ARDS in Pediatric Burn Patients: A Prospective Evaluation

JUST BREATHE, Breathing Life Into Innovative Therapies for ARDS- Cohort B: Paridiprubart

Vadadustat for the Treatment of Nonintubated Acute Respiratory Distress Syndrome Due to Pathogen-Associated Lung Injury

A Trial of Staff Time With Proned Patients in the ICU Using the 'BathMat'

RecruitmEnt Assessed by eleCtRical Impedance Tomography

Clinical Evaluation of a Point of Care (POC) Assay to Identify Phenotypes in the Acute Respiratory Distress Syndrome