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We Compared the Covid-19 Acute Respiratory Distress Syndrome (ARDS) Patients Who Applied Prone Positioning for16-24 Hours vs 24-48 Hours

NCT ID: NCT06530095

Last Updated: 2024-07-31

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

350 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-10-03

Study Completion Date

2024-02-15

Brief Summary

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The goal of this study is to understand if there is any improvement on oxygenation of patients diagnosed with Covid-19 ARDS patients when we extend the duration of prone positioning.

Second outcome of the study is to investigate mortality of patients when we extend the duration of prone positioning.

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Detailed Description

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Conditions

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Morality Oxygenation Indices Hypoxia

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

RETROSPECTIVE

Study Groups

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Group A

Patients who have been in prone positioning for 16-24 hours

prone positioning

Intervention Type OTHER

prone positioning

Group B

Patients who have been in prone positioning for 24-48 hours

prone positioning

Intervention Type OTHER

prone positioning

Interventions

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prone positioning

prone positioning

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

COVİD 19 ARDS patients patients who have been intubated for 48 hours and more

Exclusion Criteria

Pediatric patients Patients who extubated in less than 48 hours Patients with Lung and pleural malignancies
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Bakirkoy Dr. Sadi Konuk Research and Training Hospital

OTHER_GOV

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Bakirkoy Dr Sadi konuk Research and Training hospital

Istanbul, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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2022/318

Identifier Type: -

Identifier Source: org_study_id

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