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Biobank Glioma: Storing Blood for Analysis of DNA and Protein of Patients With Glioma
This study is currently recruiting participants.
Verified by Maastricht Radiation Oncology, April 2007
Sponsors and Collaborators: Maastricht Radiation Oncology
Maastricht University Medical Center
Information provided by: Maastricht Radiation Oncology
ClinicalTrials.gov Identifier: NCT00181493
  Purpose

The purpose of this study is to determine, by means of DNA and protein analysis, the relationship between DNA and protein profiles and a number of endpoints which are important for the patient with glioma, such as over all survival and side effects.


Condition
Glioma

U.S. FDA Resources
Study Type: Observational
Study Design: Screening, Longitudinal, Random Sample, Prospective Study
Official Title: Storing Blood for Analysis of DNA and Protein of Patients With Glioma in MAASTRO Clinic

Further study details as provided by Maastricht Radiation Oncology:

Estimated Enrollment: 99
Study Start Date: March 2003
Estimated Study Completion Date: January 2025
Detailed Description:

It has already been known for a long time that cancer is a genetic disorder and that the development of the illness is a very complex interaction between genetic and surrounding factors. Also the response on therapy and the development and seriousness of side effects is stipulated by this complicated collaboration of genetic and surrounding factors. Moreover it is not only the DNA that plays an important role but also the systems of control at the protein level. At this moment a lot of questions remain to be answered because up till now the studies were of rather restricted statistical strength with frequently inconsistent dates and moreover retrospective. Major retrospective studies are necessary to distinguish the relationship between DNA/protein patterns and clinically relevant endpoints like prognosis and toxicity in which an as broad as possible patient group is being monitored. For this reason we want to draw blood in the MAASTRO clinic of all patients with glioma and store it encrypted so that we can perform DNA and protein analyses in the future and to correlate the results with survival and toxicity of the treatment.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Glioma brain tumor

Exclusion Criteria:

  • Not able to comply with follow-up
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00181493

Contacts
Contact: Philippe Lambin, Prof, PHD +31 (0) 88 44 55 666 philippe.lambin@maastro.nl
Contact: Dirk De Ruysscher, PHD +31 (0) 88 44 55 666 dirk.deruysscher@maastro.nl

Locations
Netherlands, Limburg
Maastricht Radiation Oncology Recruiting
HEERLEN, Limburg, Netherlands, 6419 PC
Contact: Dirk De Ruysscher, PHD     +31 (0) 88 44 55 666     dirk.deruysscher@maastro.nl    
Contact: Brigitta Baumert, PHD     +31 (0) 88 44 55 666     brigitta.baumert@maastro.nl    
Sponsors and Collaborators
Maastricht Radiation Oncology
Maastricht University Medical Center
Investigators
Principal Investigator: Brigitta Baumert, PHD MAASTRO-clinic
  More Information

Study ID Numbers: P03.0321L
Study First Received: September 12, 2005
Last Updated: April 24, 2007
ClinicalTrials.gov Identifier: NCT00181493  
Health Authority: Netherlands: The Central Committee on Research Involving Human Subjects (CCMO)

Keywords provided by Maastricht Radiation Oncology:
Glioma
genomics
proteomics

Study placed in the following topic categories:
Neuroectodermal Tumors
Neoplasms, Germ Cell and Embryonal
Neuroepithelioma
Glioma
Neoplasms, Glandular and Epithelial

Additional relevant MeSH terms:
Neoplasms
Neoplasms by Histologic Type
Neoplasms, Nerve Tissue
Neoplasms, Neuroepithelial

ClinicalTrials.gov processed this record on January 16, 2009