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

No results posted yet for this study

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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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06877884 on ClinicalTrials.gov