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Clinical Trials/NCT02303353
NCT02303353
Unknown
Not Applicable

Data Base Project for Acquisition of Cancer Patient Data in Practices and Ambulant Therapy

SPGO Research Mannheim GmbH1 site in 1 country2,000 target enrollmentOctober 2013
ConditionsCarcinoma

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Carcinoma
Sponsor
SPGO Research Mannheim GmbH
Enrollment
2000
Locations
1
Primary Endpoint
Anti-cancer treatments (Course of the disease and type of applied anti-cancer therapies. Assessment of guidelines' implementation)
Last Updated
9 years ago

Overview

Brief Summary

The purpose of this registry is to evaluate the situation regarding ambulant therapy of cancer patients in different practices in Germany. It should provide insight into the implementation of schemes for cancer therapy predefined in the guidelines, the treatment of diverse adverse reactions and the counter measures taken. Thereby, potential differences in treatment and with that differences in quality amongst individual practices might be identified. The medium to long term aim is to contribute to positively influence the quality of medical care of cancer patients in Germany.

Registry
clinicaltrials.gov
Start Date
October 2013
End Date
September 2018
Last Updated
9 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
SPGO Research Mannheim GmbH
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • 18 years and older
  • Tumor disease (carcinoma of either breast, ovary, lung, colon, stomach, pancreas, rectum or plasmacytoma)
  • Written informed consent

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Anti-cancer treatments (Course of the disease and type of applied anti-cancer therapies. Assessment of guidelines' implementation)

Time Frame: From date of ICF until date of cure/death/ICF withdrawal, up to 60 months

Course of the disease and type of applied anti-cancer therapies. Assessment of guidelines' implementation

Secondary Outcomes

  • Adverse reactions and their treatment (Number and type of adverse reactions and applied counter measures / therapies)(From date of ICF until date of cure/death/ICF withdrawal, up to 60 months)

Study Sites (1)

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