Actively Recruiting
Radiation Oncology Registry and Biosample Repository for Patients with Cancer or Benign Tumors
Led by Abramson Cancer Center at Penn Medicine · Updated on 2026-03-04
8000
Participants Needed
4
Research Sites
1174 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to create a registry and collect biosamples from patients diagnosed with cancer or benign tumors who are receiving radiotherapy. The purpose is to gather valuable data and biological specimens to support future studies related to these conditions. Participants will provide samples such as blood, urine, and tumor tissue as part of this process. The study involves collecting and storing these biosamples alongside clinical information to build a comprehensive repository. Participants will be followed for health assessments over a period of 10 years. Throughout this time, researchers will monitor and evaluate health outcomes related to the participants' cancer or tumor diagnoses and treatments.
CONDITIONS
Official Title
The Radiation Oncology Registry and Biosample Repository
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years or older
- Diagnosis of cancer and/or benign tumor
- Currently undergoing radiotherapy
- Able to provide informed consent
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
AI-Screening
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Trial Site Locations
Total: 4 locations
1
Virtua Samson Cancer Center
Moorestown, New Jersey, United States, 08057
Not Yet Recruiting
2
Virtua Health & Wellness Center
Voorhees Township, New Jersey, United States, 08043
Actively Recruiting
3
Lancaster General Hospital
Lancaster, Pennsylvania, United States, 17604
Actively Recruiting
4
University of Pennsylvania
Philadelphia, Pennsylvania, United States, 19104
Actively Recruiting
Research Team
P
Project Manager
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
Frequently Asked Questions
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