UPCC 11908 Registry and Biosample Repository
Registry and Biosample Repository in Patients Undergoing Radiotherapy
Brief description of study
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.
Eligibility of study
You may be eligible for this study if you meet the following criteria:
- Conditions: Neoplasia
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Age: 18 years or above
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Gender: All
- Anyone age 18 and above with a cancer and/or benign tumor diagnosis undergoing
radiotherapy
- Able to sign consent
This study investigates the creation of a registry and biosample repository for patients diagnosed with cancer or benign tumors who are undergoing radiotherapy. A biosample repository includes biological samples such as blood, urine, and tumor specimens, which are collected and stored for research purposes.
Participants in this study will have their blood, urine, and tumor samples collected while they undergo their routine radiotherapy treatment. These samples will be stored in a repository to help researchers understand more about cancer and benign tumors.
- Who can participate: Individuals aged 18 and above with a diagnosis of cancer or benign tumors who are undergoing radiotherapy can participate. Participants must be able to sign consent.
- Study details: Participants will provide blood, urine, and tumor samples during their radiotherapy treatment. These samples will be used for research purposes and stored in a biosample repository.
Study is selecting its participants from a population, or group of people, decided on by the researchers in advance.
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