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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03753841
Other study ID # GI 208/16-1
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 14, 2014
Est. completion date September 16, 2016

Study information

Verified date November 2018
Source University of Giessen
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Dysphagia is associated with high rates of mortality and morbidity. Adjusting the oral diet of ICU-patients based on flexible endoscopic evaluation of swallowing (FEES) findings might reduce pneumonia rate, mortality and need for intubation/tracheotomy.


Description:

Dysphagia, a common complication in neurological disorders, leads to high rates of mortality and morbidity. It is prevalent in critically ill patients, especially those who need mechanical ventilation. The investigators therefore investigate the effect of adjusting the oral diet of our intensive care unit (ICU) patients based on flexible endoscopic evaluation of swallowing (FEES) findings, thereby assessing the impact of FEES on a neurological ICU. All patients treated on the investigators neurological ICU will be eligible for this study.

The investigators will correlate findings with baseline data, disability status, pneumonia and duration of hospitalisation, as well as a need for mechanical ventilation or a tracheotomy.


Recruitment information / eligibility

Status Completed
Enrollment 125
Est. completion date September 16, 2016
Est. primary completion date September 3, 2016
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Treatment on neurological ICU

- Clinical suspicion of Dysphagia

Exclusion Criteria:

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Adjustment of oral diet
Adjustment of oral diet based on findings in fiberendoscopic evaluation of swallowing (FEES)

Locations

Country Name City State
Germany Universitätsklinikum Gießen Gießen Hessen

Sponsors (1)

Lead Sponsor Collaborator
University of Giessen

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pneumonia Rate self-explanatory Up to 130 days
Primary Mortality self-explanatory Up to 130 days
Secondary Length of stay in hospital self-explanatory Up to 130 days
Secondary Intubation/Tracheotomy Rate of Intubation/Tracheotomy Up to 130 days
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