The goal of this clinical trial is to better understand how ctDNA can help with early detection and monitoring of patients diagnosed with cancer in Oklahoma City, OK and help in improving personalized treatment strategies.
Join our trials for patients diagnosed with cancer in Oklahoma City, OK where your participation in the blood samples collection from cancer patients can help advance our understanding of cancer and its potential treatment options.
Cancer characterizes uncontrolled cell growth in various body parts that can also spread to other sites. It affects millions of people yearly. There is a dire need to better understand how cancer works and then ultimately explore effective therapeutic interventions and give hope to those suffering.
Hightower Clinical is conducting research studies for patients diagnosed with cancer in Oklahoma City, OK. This study is a non-interventional, multi-center research involving cancer patients. Participants will have plasma ctDNA biomarker testing at certain times during their regular treatment to help track and understand the disease better.
*Joining the clinical trial is free and entirely your choice.
*Simply fill out the form, and our research team member will reach out to check if you’re eligible for the study.
Study Name | Protocol Number | Sponsor |
---|---|---|
Cancer Bio Repository | Tempus |
In order to profile longitudinal ctDNA biomarker at specific time points, Hightower Clinical is conducting biorepository clinical trials for patients diagnosed with cancer in Oklahoma City, OK.
This clinical trial is meant for monitoring and diagnosing biomarkers in cancer patients. It is a non-interventional, multicenter, multicohort monitoring of cancer patients. Patients will undergo a detection test from time to time for longitudinal plasma ctDNA biomarker profiling. Parallel to it, they will be given standard care therapy.
This study enrolls participants diagnosed with cancer willing to provide additional blood samples for ctDNA research.
*All study procedures and treatments, including the investigational drug, are provided at no cost, and insurance is not needed to join.
*The study doctor will guide you through each step of the clinical trial, answering any questions you may have about the treatment before you decide to participate.
When you agree to enroll in the study, you will be asked to sign an Informed Consent Form (ICF). The ICF delves into the details of the study. Our research team will guide you through the process and explain your role in the trial. We encourage you to ask as many questions as you need before deciding whether to participate or withdraw.
After signing the consent form and addressing your concerns, you will be monitored regularly for biomarker profiling through expert professionals.
This study does not involve any additional treatments. It takes place across multiple centers and includes different groups of cancer patients. The participants will have their blood tested for ctDNA biomarkers at specific time intervals while they continue with their regular cancer treatment.
Study-related care is provided at no cost, and you will be supervised via experienced doctors and healthcare professionals conducting thorough exams and assessments.
18 Years to 99 Years (Adult, Older Adult)
All
Cancer
Recruiting
Cancer represents the condition when abnormal cells begin to multiply uncontrollably, forming tumors or spreading to other body parts. These cells can invade surrounding tissues, disrupting the normal functioning of organs and systems.
The goal of this clinical trial is to better understand how ctDNA can help with early detection and monitoring of patients diagnosed with cancer in Oklahoma City, OK and help in improving personalized treatment strategies.
Participating in this study, you can contribute to groundbreaking research that could lead to more effective cancer treatments. Additionally, you may also benefit from personalized insights into your own cancer’s genetic makeup.
ctDNA is collected through a simple blood test, and then analyzed in a lab to look for genetic markers that can help guide cancer treatment decisions.
ctDNA profiling might provide additional insights into your cancer, but any changes to your treatment plan would be discussed with your doctor based on the findings.
The risks are minimal, mainly related to the blood drawn itself. However, your healthcare team will monitor you closely throughout the study to ensure your safety.