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A Prospective Registry to Enable Collection of Standardized Routine Care Oncology Patient Data

N

N-Power Medicine

Status

Enrolling

Conditions

Cancer

Study type

Observational

Funder types

Industry

Identifiers

NCT06877884
NPM-001

Details and patient eligibility

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

20,000 estimated patients

Sex

All

Ages

18 to 120 years old

Volunteers

Accepts Healthy 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

Trial contacts and locations

7

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Central trial contact

Louise Polychronopoulos, PhD; Christer Svedman, MD

Data sourced from clinicaltrials.gov

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