Frequently Asked Questions about Clinical Trials
🩺 Questions about clinical trials in general
A clinical trial is a medical research study in which new treatments, drugs, or therapy combinations are evaluated for diseases such as cancer. Participants help researchers determine whether these treatments are safe and effective. Each trial follows a specific protocol with clear requirements on who can participate and what procedures will be performed.
Participating in a clinical trial gives you access to innovative treatments that may not otherwise be available. It also helps advance medical science and benefits future patients. In many cases, participants receive specialized medical care during the study.
Each trial has specific inclusion and exclusion criteria, which may include the type of cancer, stage of the disease, previous treatments, and health conditions. A professional at the center will review your medical history and let you know if you meet the requirements.
At our center we work with clinical trials for different types of cancer, including (but not limited to) breast, prostate, lung, colon, and hematological cancers such as lymphomas or leukemias. Availability varies depending on the open studies.
If you do not qualify for a particular trial, we will explore other available options. It is possible that in the future new studies will open for which you may be eligible. In addition, you can always continue with your standard treatment.
Yes, some studies have age limits or specific health requirements. However, there are also trials designed for older adults or people with additional medical conditions. Each case is evaluated individually.
💊 Questions about treatment
The treatment depends on the trial. It may include a new drug, a combination of therapies, or a standard treatment. All the information will be clearly explained before you decide to participate.
The treatment under study may offer additional benefits, such as greater effectiveness or fewer side effects. However, as it is still under investigation, data on its performance are still being collected.
In some studies, especially those where there is no standard treatment, a placebo may be used. However, you will never be left without treatment if there is a recognized therapeutic option. You will always be informed with transparency.
Yes. During the trial you will receive continuous medical care from a specialized team. Your health and any effects of the treatment will be monitored regularly.
Yes. You may continue with your current oncologist. Our team will collaborate with your doctor to ensure comprehensive and coordinated care.
💸 Questions about costs and logistics
Generally, no. Clinical trials usually cover investigational medications, related tests, and necessary visits. You will be clearly informed if anything is not covered.
Study sponsors (such as pharmaceutical companies or research institutions) usually cover the costs of the investigational treatment and related exams.
Not necessarily. Some trials do not require health insurance, although in other cases insurance may cover part of the standard treatment. We will help you understand the requirements of each study.
Some studies provide assistance for transportation, parking, or lodging, especially if you live far from the center. We will verify whether this support is available in the trial that interests you.
❤️ Questions about safety and well-being
Patient safety is the top priority. All studies are reviewed by ethics committees and follow strict regulations. You will be closely monitored throughout the process.
All treatments may have risks. You will be thoroughly informed about the possible side effects before starting. You will be able to ask all the questions you need.
If that happens, the medical team will evaluate your situation and decide whether the treatment should be modified or discontinued. Your well-being comes first.
Yes. Participation is completely voluntary. You may withdraw from the trial at any time, without penalty or impact on your medical treatment.
📝 Questions about the process
First, an initial evaluation is conducted to see if you qualify. Then the entire study will be explained to you and, if you decide to participate, you will sign an informed consent. After that, initial tests are performed and the treatment begins.
Depending on the study, you may need blood tests, imaging studies (such as CT or MRI), physical evaluation, among others. All of this will be detailed before starting.
The duration varies depending on the protocol. It can be from a few weeks to several months or more. You will be informed exactly how long the trial lasts before making a decision.
That will depend on the specific study. Some visits may be weekly at first and then monthly. You will receive a clear schedule of appointments and exams.
👨👩👧👦 Questions about family and caregivers
Yes. In fact, we encourage you to come accompanied if you wish. Having someone you trust can help you feel more comfortable and better understand the process.
Yes. Our team of professionals will guide you at every step. Everything will be explained calmly and all your questions will be answered before you make any decision.
Your family can accompany you to appointments, help with transportation, or communicate with the medical team if they have questions. They can also participate in informational sessions if you wish.