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NCT01974089 Clinical Trial

Oropharyngeal Dysphagia in Patients With Community Acquired Pneumonia

Pneumonia Clinical Trial

Official title:
Oropharyngeal Dysphagia in Patients With Community Acquired Pneumonia

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01974089
Other study ID # RHN_DMK_03
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 2013
Est. completion date March 2014

Study information
Verified date April 2019
Source Vendsyssel Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study investigates relationship between community acquired pneumonia and oropharyngeal dysphagia in patients admitted to a department of respiratory medicine in Northern Denmark.

The endpoints will be re-hospitalisation and mortality.

Description:

Community acquired pneumonia (CAP) is an important cause of morbidity and mortality in elderly patients. Risk factors are many including oropharyngeal dysphagia (OD). Systematic screening of OD is recommended for at-risk popolations, however these resommandations do not specifically address elderly patients hospitalized with CAP.

In this study OD is assessed in all patients by Volume-Viscosity Swallowing Test (V-VST) The study is registered by the Danish Data Protection Authority (2008-58-0028)

Recruitment information / eligibility
Status Completed
Enrollment 154
Est. completion date March 2014
Est. primary completion date October 2013
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Temperature > 38 degrees Celcius

- New infiltrate on chest x-ray

- Increased C-reactive protein (CRP)

- Either cough, dyspnea, pleuritic chest pain, expectoration, or tachypnea

Exclusion Criteria:

- patients referred from the intensive care unit

- reduced cognitive awareness if not able to able to cooperate with the assessment of oropharyngeal dysphagia

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Dysphagia
Oropharyngeal dysphagia assessed by Volume-Viscosity Svallowing Test

Locations
Country Name City State
Denmark Vendsyssel Hospital Hjørring

Sponsors (1)
Lead Sponsor Collaborator
Vendsyssel Hospital

Country where clinical trial is conducted

Denmark, 

Outcome
Type Measure Description Time frame Safety issue
Primary Intra Hospital Mortality Intra hospital mortality is death while the patient is hospitalized With in 10 days from admission
Primary 30 Day Mortality Death within 30 days of discharge 30 days after discharge
Primary Re-hospitalization The rate of re-hospitalization within 30 days of discharge 30 days after discharge
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