Clinical trial Recruiting at 7 sites Observational Ages 18 to 120

Registry for collecting oncology patient data

Official title: A Prospective Registry for Collecting Standardized, Routine Care Data to Characterize Patients, Treatment Patterns, Safety and Treatment Effectiveness in Adult Oncology Patients

Run by N-Power Medicine · NCT06877884 · Data updated 2026-11-12

This study is collecting information from cancer patients to help improve research and make it easier for them to join clinical trials.

Quick facts

Study typeObservational
Ages18 Years to 120 Years
SexAll
Enrollment20000 (estimated)
SponsorN-Power Medicine
Industry-sponsored
Locations7 sites (Monterey, California and 6 other locations)
StatusRecruiting
StartedAugust 1, 2022
Main results expectedJanuary 2099
Study endsJanuary 2099
Registry record updatedOctober 20, 2025
Trial IDNCT06877884 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adult patients (18 years and older) receiving care at participating oncology centers who can provide informed consent.

Probably not a fit

Patients who are prisoners or unable to consent without a legally authorized representative may not benefit from this registry.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational registry collects standardized data from patients at various oncology centers. It includes information on baseline variables, treatments administered, and patient-reported outcomes through surveys. The goal is to create a comprehensive database that can facilitate patient participation in clinical trials and enhance research and development in oncology.

Why it matters

Potential benefit: If successful, this registry could improve the understanding of cancer treatments and outcomes, leading to better patient care and more effective clinical trials.

How similar studies have gone: Other observational registries in oncology have shown success in improving data collection and patient engagement, making this approach promising.

Who can join: the full rules

Show full inclusion / exclusion criteria
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

Where it's running

  • Pacific Cancer Care
    Monterey, California, United States
    Recruiting
  • Bayhealth Cancer Center-Kent
    Dover, Delaware, United States
    Recruiting
  • Bayhealth Cancer Center- Sussex
    Milford, Delaware, United States
    Recruiting
  • Northwest Oncology & Hematology
    Elk Grove Village, Illinois, United States
    Recruiting
  • New Mexico Oncology Hematology Consultants
    Albuquerque, New Mexico, United States
    Recruiting
  • Lankenau Medical Center
    Paoli, Pennsylvania, United States
    Recruiting
Show 1 more location
  • Oncology Consultants, P.A.
    Houston, Texas, United States
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

  • External control arm registry for non-small cell lung cancer

    This project will build control groups from current and future clinical and registry data to help compare treatments for adults with non-small cell lung cancer.

    Recruiting at 11 sites N-Power Medicine · Monterey, California and 10 other locations · NCT07174388

  • Prospective external control cohort for newly diagnosed advanced EGFR‑mutant NSCLC

    This project will create a prospective group of people with newly diagnosed advanced EGFR‑mutant non‑small cell lung cancer to collect standardized clinical and imaging data as an external control for treatment comparisons.

    Recruiting at 9 sites N-Power Medicine · Monterey, California and 9 other locations · NCT07028489

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
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Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.