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NCT02247947 Clinical Trial

Proteomics to Identify Prognostic Markers After CPR and to Estimate Neurological Outcome

Cardiac Arrest Clinical Trial

Official title:
Proteomics to Identify Prognostic Markers After CPR and to Estimate Neurological Outcome

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02247947
Other study ID # 14-053
Secondary ID
Status Completed
Phase
First received
Last updated
Start date September 2014
Est. completion date November 1, 2020

Study information
Verified date November 2020
Source Universitätsklinikum Köln
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Proteomics is used to identify prognostic markers after CPR. Additionally neurological outcome should be estimated by specific protein alterations and affections of pathways.

Description:

Proteomics is used to identify prognostic markers after CPR, i.e. altered proteins on a 2G-gel. Additionally neurological outcome should be estimated by specific protein alterations and affections of pathways.

Recruitment information / eligibility
Status Completed
Enrollment 20
Est. completion date November 1, 2020
Est. primary completion date November 1, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - cardiac arrest Exclusion Criteria: - trauma

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Germany University Hospital of Cologne Cologne NRW

Sponsors (1)
Lead Sponsor Collaborator
Universitätsklinikum Köln

Country where clinical trial is conducted

Germany, 

Outcome
Type Measure Description Time frame Safety issue
Primary death at day 20 day 20
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