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Clinical Trials/NCT00889798
NCT00889798
Completed
Not Applicable

Epidemiological Registry Describing Treatment Reality and Therapy Modalities of Patients With Malignant Lymphatic Systemic Diseases (Non-Hodgkin's Lymphoma, Chronic Lymphocytic Leukemia and Multiple Myeloma) Requiring Therapy.

iOMEDICO AG0 sites3,795 target enrollmentApril 2009

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Non-Hodgkin's Lymphoma (NHL)
Sponsor
iOMEDICO AG
Enrollment
3795
Primary Endpoint
Course of treatment (treatment reality)
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

The purpose of this registry is to record information on therapy reality of malignant lymphatic systemic diseases by office-based haematologists in Germany.

Detailed Description

The TLN is a prospective, longitudinal, nation wide cohort study with the purpose to record information on the antineoplastic treatment of lymphatic neoplasms in Germany. The registry will follow patients for up to five years. It will identify common therapeutic sequences and changes in the treatment of the disease. At inclusion, data in patient characteristics, comorbidities, tumor characteristics and previous treatments are collected. During the course of observation data on all systemic treatments, radiotherapies, surgeries, and outcome are documented. The impact of nutrition (LyNut) and physical activity (LyNut) on the course of the adjuvant disease will be examined in patients with indolent and aggressive Non-Hodgin Lymphoma, as well as long-term effects of systemic treatment (LyTox) and quality of life (LyLife) in patients with multiple myeloma.

Registry
clinicaltrials.gov
Start Date
April 2009
End Date
August 31, 2019
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Confirmed diagnosis of Non-Hodgkin's lymphoma, chronic lymphocytic leukaemia or multiple myeloma
  • Must receive a first- or second-line therapy
  • 18 years or older
  • Signed, written informed consent

Exclusion Criteria

  • no systemic therapy

Outcomes

Primary Outcomes

Course of treatment (treatment reality)

Time Frame: 5 years per patient

Documentation of anamnestic data and therapy sequences

Secondary Outcomes

  • Effectiveness of treatment(5 years per patient)

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