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About
This is an observational registry for patients at participating oncology centers. The data collection includes but is not limited to baseline variables, treatments given and outcome data. Patient surveys are also included. The aim of the study is to generate rich and standardized data for patients and to help enable more patients participate in clinical trials and contribute to research and development.
Full description
This is an observational registry for patients at participating oncology centers. The data collection includes but is not limited to baseline variables, treatments given and outcome data. Patient surveys are also included. The aim of the study is to generate rich and standardized data for patients and to help enable more patients participate in clinical trials and contribute to research and development.
Enrollment
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Volunteers
Inclusion criteria
Be a patient at a site (oncology) participating in the Registry Be at least 18 years old Be able and willing to provide signed informed consent
Exclusion criteria
Prisoners/imprisonment at time of screening for eligibility Patients who cannot consent without utilization of a legally authorized representative
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Central trial contact
Louise Polychronopoulos, PhD; Christer Svedman, MD
Data sourced from clinicaltrials.gov
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