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Mediators of Inflammation, Prognostic Markers and Genetic Polymorphisms in Patients With Sepsis (MaSep)

The recruitment status of this study is unknown because the information has not been verified recently.
Verified February 2012 by Universitätsmedizin Mannheim.
Recruitment status was  Recruiting
Information provided by (Responsible Party):
Dr. med. Ursula Hoffmann, University Hospital Mannheim Identifier:
First received: February 14, 2012
Last updated: February 16, 2012
Last verified: February 2012

During the past years many investigators have focused on the immunological changes in sepsis disease, and great attention has been paid to the development of practicable means of immunomonitoring. Little is known about diagnostic and prognostic vascular biomarkers during the time course of patients with sepsis.


Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Evaluation of Mediators of Inflammation, Prognostic Markers and Genetic Polymorphisms in Patients With Sepsis

Resource links provided by NLM:

Further study details as provided by Universitätsmedizin Mannheim:

Biospecimen Retention:   Samples Without DNA

Peripheral blood samples

Estimated Enrollment: 300
Study Start Date: January 2012
Estimated Study Completion Date: January 2015
Detailed Description:

Primary Outcome Measures:

New diagnostic and prognostic markers for septic patients

Estimated Enrollment: 300 patients Study Start Date: January 2012 Estimated Study Completion Date: open Estimated Primary Completion Date: open

Intervention Details:

Procedure: vein puncture comparison of different inflammatory markers in the blood of septic patients


Ages Eligible for Study:   18 Years to 90 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Sampling Method:   Probability Sample
Study Population

Patients suffering from sepsis


Inclusion Criteria:

  • SIRS-Criteria
  • Proven Infection
  • One sepsis-induced organ-failure
  • Adults < 18 years old

Exclusion Criteria:

  • Anemia
  • Pregnancy
  • Blood donor in the last 3 month
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its identifier: NCT01535534

University Medical Centre Mannheim Recruiting
Mannheim, Baden-Württemberg, Germany, 68167
Contact: Ursula Hoffmann, MD    00496213832030   
Contact: Michael Behnes, MD    00496213832030   
Sponsors and Collaborators
Universitätsmedizin Mannheim
Principal Investigator: Ursula Hoffmann, MD Universitätsmedizin Mannheim
Study Director: Michael Behnes, MD Universitätsmedizin Mannheim
  More Information

No publications provided

Responsible Party: Dr. med. Ursula Hoffmann, Principal Investigator, University Hospital Mannheim Identifier: NCT01535534     History of Changes
Other Study ID Numbers: 2011-384N-MA
Study First Received: February 14, 2012
Last Updated: February 16, 2012
Health Authority: Germany: Federal Institute for Drugs and Medical Devices

Keywords provided by Universitätsmedizin Mannheim:

Additional relevant MeSH terms:
Pathologic Processes
Systemic Inflammatory Response Syndrome processed this record on March 02, 2015