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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01162161
Other study ID # Sphingo-AC
Secondary ID
Status Completed
Phase N/A
First received July 13, 2010
Last updated September 22, 2015
Start date July 2010
Est. completion date May 2013

Study information

Verified date September 2015
Source RWTH Aachen University
Contact n/a
Is FDA regulated No
Health authority Germany: Ethics Committee
Study type Observational

Clinical Trial Summary

In this mono-center prospective study, the impact of changes in the sphingolipid metabolism in patients with pulmonary edema will be investigated.


Description:

There will be three groups of patients:

1. hydrostatic pulmonary edema

2. toxic pulmonary edema

3. not ventilated patients without any pulmonary edema

Samples of a routine bronchoalveolar lavage and EDTA-blood will be analysed in respect of sphingolipids, ceramide, sphingomyelin-phosphodiesterase and several cytokines.


Recruitment information / eligibility

Status Completed
Enrollment 45
Est. completion date May 2013
Est. primary completion date December 2012
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- above the age of 18

Exclusion Criteria:

- taking steroids

Study Design

Observational Model: Case-Crossover, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Germany Medical Clinic I, University Hospital Aachen Aachen Nordrhein-Westfalen

Sponsors (1)

Lead Sponsor Collaborator
RWTH Aachen University

Country where clinical trial is conducted

Germany, 

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