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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03487510
Other study ID # DICE
Secondary ID
Status Completed
Phase
First received
Last updated
Start date November 11, 2017
Est. completion date May 1, 2018

Study information

Verified date May 2018
Source University Hospital Inselspital, Berne
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Recording of routine practice patterns to detect and/or treat Dysphagia on the ICU via interview of local colleagues. This will not allow to record generalizable data, but will reflect the actual routine standard of care.


Recruitment information / eligibility

Status Completed
Enrollment 49
Est. completion date May 1, 2018
Est. primary completion date May 1, 2018
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion criteria:

- All senior ICU physicians in charge for adult critically ill ICU patients. Respective ICUs must be accredited by the "Schweizerische Gesellschaft für Intensivmedizin".

- ICUs located in Switzerland.

- Senior ICU physicians willing to voluntarily fill in the provided questionnaire.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
NO interventions apply
does not apply

Locations

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

Sponsors (1)

Lead Sponsor Collaborator
University Hospital Inselspital, Berne

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of centers using fibre-optic endoscopic evaluation of swallowing (FEES) vs. non-instrumental methods to detect/ treat dysphagia on the ICU. Analysis of number of ICUs using instrumental methods (FEES) vs. non-instrumental methods in local (Swiss) centers to detect dysphagia in the ICU. through study completion, an average of 1 month
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