A Prospective Registry to Enable Collection of Standardized Routine Care Oncology Patient Data
NCT06877884 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 20000
Last updated 2025-10-20
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.
Conditions
Sponsors & Collaborators
-
N-Power Medicine
lead INDUSTRY
Eligibility
- Min Age
- 18 Years
- Max Age
- 120 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2022-08-01
- Primary Completion
- 2099-01-31
- Completion
- 2099-01-31
Countries
- United States
Study Locations
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