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OpenTrials
Recruiting

NCT Number: NCT06877884

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

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.

Recruiting

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Key information

Conditions

Cancer Neoplasms

Age range

18 year–120 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Pacific Cancer Care, Monterey, California, United States

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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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Primary outcomes

  1. Treatment Effectiveness - Time to treatment discontinuation

    Time frame: This is an open-ended registry where data will be collected, analysed and presented regularly over time.

    Effectiveness outcomes of treatments used in routine clinical care (such as for instance time to treatment discontinuation ) will be captured

Study contacts

Contact information is provided by the study sponsor or research team.

Christer Svedman, MD

CONTACT

[email protected]

833-467-6734

Louise Polychronopoulos, PhD

CONTACT

[email protected]

833-467-6734

Sponsors and collaborators

Lead sponsor

N-Power Medicine

Industry

Registry information

Official study title

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

Important dates

Study start
2022
Primary completion
2099
Study completion
2099
First posted
Mar 14, 2025
Registry last updated
Oct 20, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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