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

Recruiting now

Conditions studied: Cancer

In brief

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.

Key facts

Study ID

NCT06877884

Run by

N-Power Medicine

People needed

20000

Starts

2022-08-01

Expected to finish

2099-01-01

Last updated by the study team

2025-10-20

Who can join

Age: 18 and older, up to 120. Sex: any. Healthy volunteers: accepted.

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 is running

• Pacific Cancer Care — Monterey, California, United States (enrolling)
• Bayhealth Cancer Center-Kent — Dover, Delaware, United States (enrolling)
• Bayhealth Cancer Center- Sussex — Milford, Delaware, United States (enrolling)
• Northwest Oncology & Hematology — Elk Grove Village, Illinois, United States (enrolling)
• New Mexico Oncology Hematology Consultants — Albuquerque, New Mexico, United States (enrolling)
• Lankenau Medical Center — Paoli, Pennsylvania, United States (enrolling)
• Oncology Consultants, P.A. — Houston, Texas, United States (enrolling)

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.