Cancer
Conditions
Brief summary
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.
Detailed 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.
Interventions
None listed
Sponsors
N-Power Medicine
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to 120 Years
Healthy volunteers
Yes
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
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Treatment Effectiveness - Time to treatment discontinuation | This is an open-ended registry where data will be collected, analysed and presented regularly over time. | Effectiveness outcomes of treatments used in routine clinical care (such as for instance time to treatment discontinuation ) will be captured |
Countries
United States
Contacts
Primary ContactChrister Svedman, MD
Backup ContactLouise Polychronopoulos, PhD
Outcome results
None listed