Actively Recruiting
Development of a Biological Database in the Field of Operative Intensive Care
Led by RWTH Aachen University · Updated on 2019-09-18
99999999
Participants Needed
1
Research Sites
1717 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The storage and use of biomaterial samples is an important requirement for accompanying research and the acquisition of new knowledge to improve prognosis and therapy. Biobanking is explicitly recommended in official guidelines. In order to preserve the biomaterial, the patient must consent to the removal, transfer and storage of the biomaterial separately from the consent to the register. The biomaterial is taken at times at which a blood or urine sampling takes place anyway in the clinical routine. Therefore no additional interventions are necessary.
CONDITIONS
Official Title
Development of a Biological Database in the Field of Operative Intensive Care
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients after admission to the intensive care unit
- 18 years or older
- Signed informed consent
You will not qualify if you...
- No exclusion criteria are formulated; patients with multiple comorbidities, organ dysfunctions, and those not suitable for curative therapy can participate
- Palliative treatment or best supportive care decisions do not exclude participation
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Uniklinik RWTH Aachen
Aachen, Germany, 52074
Actively Recruiting
Research Team
C
Christina Kalvelage, M. Sc.
CONTACT
C
Christian Stoppe, Dr. med.
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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