ClinicalTrials.Veeva

Menu

Evaluation of Sedation in COVID-19 ARDS

G

Goethe University

Status

Completed

Conditions

Prone Position
Pulmonary Ventilation
Severe Acute Respiratory Syndrome Coronavirus 2
Hypnotics and Sedatives

Treatments

Other: Treatment group

Study type

Observational

Funder types

Other

Identifiers

NCT04667936
#20-643 -Sed II

Details and patient eligibility

About

This study focuses on the evaluation of various factors repeatedly discussed in relation to the impaired sedation of intubated ventilated COVID-19 patients. The sedation response of >100 moderately to severely affected COVID-19 ARDS was evaluated. The sedation level was measured at the bedside using the Richmond Agitation and Sedation Scale and ventilator synchrony. The evaluation was performed according to the static evaluation plan with respect to age, storage therapy and organ failure.

Enrollment

114 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

moderate to severe COVID-19 ARDS

Exclusion criteria

None

Trial design

114 participants in 1 patient group

moderate to severe COVID-19 ARDS
Description:
patients with an oxygenation index \<200 under intubation anesthesia and mechanical ventilation.
Treatment:
Other: Treatment group

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems