999999 Participants Needed

Data Repository for Cancer Research

(iCaRe2 Trial)

Recruiting at 53 trial locations
WG
MD
MM
KC
MS
Overseen ByMason Savine
Age: 18+
Sex: Any
Trial Phase: Academic
Sponsor: University of Nebraska
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial aims to gather data and biological samples from cancer patients, individuals at risk of developing cancer, and healthy individuals. The goal is to study cancer risk factors and develop new methods for prevention, detection, and treatment. Various hospitals and cancer centers, particularly in smaller and rural areas, collaborate in this effort. This trial suits those who have had cancer, are at risk for cancer, or are healthy and willing to contribute as controls. Participants must be able to consent and communicate in English or Spanish. As an unphased trial, this study offers participants the chance to contribute to groundbreaking research that could lead to significant advancements in cancer prevention and treatment.

Why are researchers excited about this trial?

Researchers are excited about the Integrated Cancer Repository for Cancer Research trial because it aims to revolutionize how we study cancer by creating a comprehensive database that integrates genetic, clinical, and treatment data from cancer patients. Unlike current methods that often rely on fragmented data, this approach provides a holistic view, potentially uncovering new insights into cancer progression and treatment responses. By enabling researchers to analyze vast amounts of data in an integrated manner, this trial could lead to more personalized and effective cancer therapies, ultimately improving outcomes for patients.

Who Is on the Research Team?

QL

Quan Ly, MD

Principal Investigator

University of Nebraska

Are You a Good Fit for This Trial?

Inclusion Criteria

I have been diagnosed with or have a history of cancer.
I am at risk for cancer or have suspicious symptoms.
I can understand and agree to the study's details.
See 3 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Data Collection

Collection and banking of blood, DNA, and urine samples for future analysis

Indefinite

Registry Development

Development and implementation of a web-based Cancer Collaborative Registry

Indefinite

Follow-up

Participants are monitored for safety and effectiveness after treatment

50 years

What Are the Treatments Tested in This Trial?

Find a Clinic Near You

Who Is Running the Clinical Trial?

University of Nebraska

Lead Sponsor

Trials
563
Recruited
1,147,000+
Unbiased ResultsWe believe in providing patients with all the options.
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