Characteristics of Weaning From Mechanical Ventilation in COVID-19 (CovWean)
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The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
ClinicalTrials.gov Identifier: NCT05049200 |
Recruitment Status :
Completed
First Posted : September 20, 2021
Last Update Posted : November 1, 2021
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Condition or disease |
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Respiration, Artificial COVID-19 |

Study Type : | Observational [Patient Registry] |
Actual Enrollment : | 326 participants |
Observational Model: | Cohort |
Time Perspective: | Prospective |
Target Follow-Up Duration: | 5 Months |
Official Title: | Epidemiology of Weaning From Invasive Mechanical Ventilation in COVID-19. Observational and Multicenter Study. |
Actual Study Start Date : | April 1, 2020 |
Actual Primary Completion Date : | August 31, 2020 |
Actual Study Completion Date : | October 1, 2020 |

- weaning rate [ Time Frame: on day 28 ]percentage of successfully weaned patients
- weaning classification [ Time Frame: on day 28 ]number of spontaneous breathing tests and days from first spontaneous breathing test to success or death
- mechanical ventilation days [ Time Frame: on day 28 ]duration of invasive mechanical ventilation
- length of ICU stay [ Time Frame: on day 28 ]days of hospitalization in ICU

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Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Sampling Method: | Non-Probability Sample |
Inclusion Criteria:
- Diagnosis of COVID-19 by PCR +
- Invasive mechanical ventilation for more than 12 hours
Exclusion Criteria:
- Subjects admitted to pediatric ICUs and surgery recovery room.
- Patients who were readmitted and required a new cycle of invasive mechanical ventilation after having been successfully weaned and released from the hospital.

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT05049200
Argentina | |
Matias Accoce | |
Pereyra, Buenos Aires, Argentina, 1894 | |
Sanatorio Anchorena de San Martin | |
San Martín, Buenos Aires, Argentina, B1650CQU |
Responsible Party: | Matias Accoce, HEAD OF RESPIRATORY THERAPY, Sanatorio Anchorena San Martin |
ClinicalTrials.gov Identifier: | NCT05049200 |
Other Study ID Numbers: |
15/16 |
First Posted: | September 20, 2021 Key Record Dates |
Last Update Posted: | November 1, 2021 |
Last Verified: | October 2021 |
Studies a U.S. FDA-regulated Drug Product: | No |
Studies a U.S. FDA-regulated Device Product: | No |
Respiration, Artificial Ventilator Weaning Airway Extubation COVID-19 |
COVID-19 Respiratory Tract Infections Infections Pneumonia, Viral Pneumonia Virus Diseases |
Coronavirus Infections Coronaviridae Infections Nidovirales Infections RNA Virus Infections Lung Diseases Respiratory Tract Diseases |