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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

Who can join

Ages 18 to 120 · All sexes · Healthy volunteers welcome

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

About the study

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.

Sponsor: N-Power Medicine · Participants: 20,000 · Started: Aug 1, 2022

Contact the study team

• Christer Svedman, MD · Phone: 833-467-6734
• Louise Polychronopoulos, PhD · Phone: 833-467-6734

Official record on ClinicalTrials.gov — NCT06877884

Locations in the U.S.

Conditions

• Cancer (all types)

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.