The Radiation Oncology Registry and Biosample Repository

Registry and Biosample Repository

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT01577251

Enrollment

8000

Registered

2012-04-13

Start date

2008-06-01

Completion date

2030-12-01

Last updated

2026-03-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neoplasia

Brief summary

The goal of this study is to establish a registry and biosample repository (defined as blood, urine, and tumor specimens) in patients with a cancer and/or benign tumor diagnosis undergoing radiotherapy.

Interventions

None listed

Study design

Observational model

OTHER

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

* Anyone age 18 and above with a cancer and/or benign tumor diagnosis undergoing radiotherapy * Able to sign consent

Design outcomes

Primary

Measure	Time frame
Health Assessments	10 years

Countries

United States

Contacts

CONTACTProject Manager

radonccru@pennmedicine.upenn.edu

PRINCIPAL_INVESTIGATORJay Dorsey, MD, PhD

University of Pennsylvania

Outcome results