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Establishment of a Tumor Bank for Tissue Samples

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Medical University of Vienna

Status

Enrolling

Conditions

Lung Neoplasms
Ovarian Neoplasms
Endocrine Gland Neoplasms
Breast Neoplasms
Neoplasms of the Female Genitalia
Colorectal Neoplasms

Treatments

Other: Collecting stool samples
Other: Sampling of ascites and pleural effusion
Other: Collecting sputum
Other: Collecting urine samples
Other: Tumor tissue collection
Other: Lavage/Irrigation
Other: Collecting saliva sample

Study type

Observational

Funder types

Other

Identifiers

NCT01789229
EK 260/2003

Details and patient eligibility

About

Establishment of a tumor bank, consisting of tissue samples of tumor patients (benign and malign tumors) and healthy people as controls. The tissue samples will be collected systematically together with the corresponding clinical data. The biological samples, the clinical date together with prospective experimental date constitute the entity of the tissue tumor bank.

This tumor bank for tissue samples, together with our tumorbank for blood samples (NCT01763125) combined constitute the entity "Tumorbank".

Full description

Recent progress in diagnosis and therapy of cancer diseases can be ascribed mainly to translational research. The relevance of "translational oncology" will only increase in the future -"From bench to bedside" - the swift implementation of new science research results in clinical studies in order to expedite progress in clinical cancer therapy for the benefit of the patient.

Its almost a matter of course in the medical science today to collect biological samples together with clinical information thereby creating the foundation for future excellent fundamental research.

The aim of this tumor bank is to consist of biological samples (together with a blood bank - see NCT01763125) and isolates of tumor patients and healthy people as controls. The biological samples, the clinical date together with prospective experimental date constitute the entity of the tumor bank. The content of the tumor bank can provide essential material for current and future research (e.g. analyses of prognostic or predictive tumor markers; genetically analysis (polymorphism, mutation, hypermethylation; verification and characterisation of disseminated tumor cells).

Enrollment

10,000 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Male/Female
  • Age 18 to 90 years max.
  • Just one current known malignant disease or just one current inflammatory disease

Exclusion criteria

  • Inflammatory disease and malignant disease
  • multiple malignancies
  • multiple diseases
  • underage

Trial design

10,000 participants in 3 patient groups

Malignant tumors
Description:
Patients who have one of the Neoplasms stated above under "conditions".
Treatment:
Other: Collecting saliva sample
Other: Lavage/Irrigation
Other: Tumor tissue collection
Other: Collecting urine samples
Other: Collecting sputum
Other: Sampling of ascites and pleural effusion
Other: Collecting stool samples
Benign controls
Description:
Patients with a benign tumor or an inflammatory disease - to be matched by age.
Treatment:
Other: Collecting saliva sample
Other: Lavage/Irrigation
Other: Tumor tissue collection
Other: Collecting urine samples
Other: Collecting sputum
Other: Sampling of ascites and pleural effusion
Other: Collecting stool samples
Healthy controls
Description:
People/patients who have no known disease at time of sampling or are admitted to the hospital for minor interventions and have no inflammatory disease.
Treatment:
Other: Collecting saliva sample
Other: Lavage/Irrigation
Other: Collecting urine samples
Other: Collecting sputum
Other: Collecting stool samples

Trial contacts and locations

3

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Central trial contact

Eva Obermayr, PhD; Robert Zeillinger, Prof.Dr.

Data sourced from clinicaltrials.gov

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