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RecruitingCancer

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

Eligible age

18–120 yrs

Accepts

All genders

Locations

6 states

Healthy volunteers

Yes

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About this 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

You may qualify if…

  • 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

You may not qualify if…

  • Prisoners/imprisonment at time of screening for eligibility Patients who cannot consent without utilization of a legally authorized representative

Where it's recruiting

California

Monterey

Delaware

Dover · Milford

Illinois

Elk Grove Village

New Mexico

Albuquerque

Texas

Houston

Source: ClinicalTrials.gov · NCT06877884 · last updated 2025-10-20

A Prospective Registry to Enable Collection of Standardized Routine Ca · TrialPath