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Recruiting

NCT Number: NCT03617939

A Lifetime Partnership With Patients Who Have or May be at Risk of Having Cancer

This is not a treatment study. The overall objective is to develop an improved standard of care through studying blood, tissue, biological, etc. samples, that patients have allowed researchers to procure.

Recruiting

Interested in participating?

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Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

University of Colorado Hospital, Aurora, Colorado, United States

Loading trial locations.

About this study

The Oncology Research Information Exchange Network (ORIEN) hopes to establish a unique collection of blood, tissue, other biological samples and their associated data (survey data, medical records data, cancer registry data, and other related data) from thousands of patients with cancer or at risk of having cancer. Their hope is to, over time, facilitate new clinical trials, technology, informatics solutions, and personalized medicine to each cancer patient.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • 18 years of age and older.
  • Diagnosed with cancer, or may be at risk for cancer.
  • Able to understand and sign the TCCP Informed Consent and Research Authorization form directly or through a legally authorized representative (LAR).

Non-English speaking subjects will also be invited to participate in the TCCP study, in accordance with COMIRB's short-form consent use.

Exclusion criteria

  • Members of vulnerable populations including neonates (birth to 30 days), children (under age 18), wards of the State, prisoners or those on probation or alternate sentencing, or decisionally challenged (adults or children that are cognitively impaired, incompetent to consent, proxy consent, or consenting in life threatening situations).

Treatment and study plan

Biospeciman Collection

Procedure

Collection of blood, tissue, and other biological samples.

Survey Assessments

Other

Data taken from patient surveys and assessments, including quality of life.

Medical Chart Reviews

Other

Data taken directly from the patients' medical charts.

Primary outcomes

  1. Improve Standard of Cancer Care

    Time frame: Up to 20 years

    Establish a longitudinal clinical and related data and tissue repository that will contain patient demographics via surveys and questionnaires.

  2. Improve Standard of Cancer Care

    Time frame: Up to 20 years

    Establish a longitudinal clinical and related data and tissue repository that will contain medical histories via surveys and questionnaires.

  3. Improve Standard of Cancer Care

    Time frame: Up to 20 years

    Establish a longitudinal clinical and related data and tissue repository that will contain cancer predisposing risk factors via surveys and questionnaires.

  4. Improve Standard of Cancer Care

    Time frame: Up to 20 years

    Establish a longitudinal clinical and related data and tissue repository that will contain quality of life care via surveys and questionnaires

  5. Improve Standard of Cancer Care

    Time frame: Up to 20 years

    Establish a longitudinal clinical and related data and tissue repository that will contain blood samples from consenting patients.

  6. Improve Standard of Cancer Care

    Time frame: Up to 20 years

    Establish a longitudinal clinical and related data and tissue repository that will contain tissue samples from consenting patients

  7. Improve Standard of Cancer Care

    Time frame: Up to 20 years

    Establish a longitudinal clinical and related data and tissue repository that will contain other biological samples from consenting patients

Study contacts

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

Kyra Anderson

CONTACT

[email protected]

303-724-3868

Sponsors and collaborators

Lead sponsor

University of Colorado, Denver

Other

Registry information

Official study title

Total Cancer Care Protocol: A Lifetime Partnership With Patients Who Have or May be at Risk of Having Cancer (ORIEN)

Important dates

Study start
2015
Primary completion
2035
Study completion
2037
First posted
Aug 7, 2018
Registry last updated
Nov 10, 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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