A Prospective Registry to Enable Collection of Standardized Routine Care Oncology Patient Data
A Prospective Registry for Collecting Standardized, Routine Care Data to Characterize Patients, Treatment Patterns, Safety and Treatment Effectiveness in Adult Oncology Patients
N-Power Medicine
20,000 participants
Aug 1, 2022
OBSERVATIONAL
Conditions
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.
Eligibility
Inclusion Criteria1
- 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 Criteria1
- Prisoners/imprisonment at time of screening for eligibility Patients who cannot consent without utilization of a legally authorized representative
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Locations(7)
View Full Details on ClinicalTrials.gov
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NCT06877884