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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03468036
Other study ID # INNOVATE
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 7, 2019
Est. completion date December 1, 2022

Study information

Verified date January 2023
Source University Hospital Inselspital, Berne
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Data analysis of routinely applied extubation procedures on the ICU: i.e. extubation with 100% O2 vs. 35% O2 with/without suctioning.


Recruitment information / eligibility

Status Completed
Enrollment 250
Est. completion date December 1, 2022
Est. primary completion date December 1, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - All adult (=18 years) ICU patients with routine extubation on the ICU during the 2-month observational interval. Exclusion Criteria: - Age < 18 years - Patients on comfort therapy and/ or terminal extubation or accidental extubationtracheostomized patients - Patients with refusal to general consent or withdrawal of general consent (DLF and/or internal database) - Patients dying without next-of-kin available

Study Design


Related Conditions & MeSH terms


Intervention

Other:
none, does not apply
none: does not apply

Locations

Country Name City State
Switzerland Dept. of Intensive Care Medicine, University of Bern, Bern

Sponsors (1)

Lead Sponsor Collaborator
Jörg Schefold

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Difference in proportion of patients with need for ongoing ventilatory support 30 days max follow-up
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