Completed
Monitoring of Lung Sounds of Patients With Pneumonia
What is being collected
Device Data
Collected from today forward - ProspectiveDevice
Who is being recruted
Infections+2
+ Lung Diseases
+ Respiratory Tract Diseases
From 18 to 90 Years
+14 Eligibility Criteria
How is the trial designed
Cohort
Tracking disease incidence in order to identify risk factors and understand disease progression over time.Observational
Study Start: April 2013
Summary
Principal SponsorRWTH Aachen University
Last updated: September 23, 2015
Sourced from a government-validated database.Claim as a partner
Study start date: April 1, 2013
Actual date on which the first participant was enrolled.The aim of this study is to investigate if any correlation between lung sounds of pneumonia patients and the clinical development or therapy of the pneumonia exists.
Principal SponsorRWTH Aachen University
Last updated: September 23, 2015
Sourced from a government-validated database.Claim as a partner
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.Design Details
17 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Cohort
These studies follow a group of individuals with common characteristics (such as a condition or birth year) over a specific period to study health outcomes or exposures.
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Conditions
Criteria
Any sex
Biological sex of participants that are eligible to enroll.From 18 to 90 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
InfectionsLung DiseasesRespiratory Tract DiseasesRespiratory Tract InfectionsPneumonia
Criteria
10 inclusion criteria required to participate
CRB-65 score > 1
CRP > 60mg/l
age at least > 18 years
ambulant aquired pneumonia with typically radiological signs
Show More Criteria
4 exclusion criteria prevent from participating
allergic reaction because of skin contact with polymers
artificial respiration or other means for supporting respiration
pneumonia acquired in a hospital
pregnancy or breast feeding
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.Treatment Groups
Study Objectives
One single intervention group is designated in this study
This study does not include a placebo group
Treatment Groups
Study Objectives
Primary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
CompletedOne Study Center