frequently asked questiONS

 A clinical trial is a research study that tests new medical treatments, devices, or therapies in people to determine their safety and effectiveness. These trials are critical to advancing medicine and finding better ways to treat or prevent diseases.

 Each clinical trial has specific eligibility criteria, which may include factors such as age, gender, medical history, and the specific condition being studied. We will assess whether you qualify during an initial screening process.

 Participant safety is our top priority. All clinical trials are conducted under strict regulatory oversight and ethical standards, including review by an Institutional Review Board (IRB) and adherence to Good Clinical Practice (GCP) guidelines. Our team closely monitors participants throughout the study to ensure their well-being.

•  Phase I: Tests the treatment’s safety and dosage in a small group of participants.
• Phase II: Expands the study to a larger group to assess effectiveness and side effects.
• Phase III: Compares the new treatment to existing treatments in a large group.
• Phase IV: Conducted after FDA approval to gather additional information on long-term effects.

Each trial has specific criteria that must be met, such as age, medical history, and current health status. We’ll conduct an eligibility screening, which may include a review of your medical records and a brief health assessment, to determine if you’re a good fit for one of our studies.

Informed consent ensures that you fully understand the details of the clinical trial, including its purpose, procedures, potential risks, and benefits. You’ll receive a document that explains the study in detail, and our team will answer any questions you have before you agree to participate.

Yes, participation is entirely voluntary. You are free to withdraw from the study at any time for any reason without any penalty or loss of benefits.

Many studies offer compensation to participants for their time, travel, and other study-related expenses. Compensation varies depending on the study and will be explained during the informed consent process.

Study visits may include physical exams, lab tests, diagnostic procedures, and treatments related to the clinical trial. The frequency and length of visits will depend on the specific study, and we’ll provide you with a detailed schedule in advance.

The length of a clinical trial varies depending on the study. Some trials may last a few weeks or months, while others can span several years. We will inform you of the study duration during the consent process.

Most clinical trials are randomized, meaning participants are assigned to either the treatment group or a control group. The control group may receive a placebo or the current standard treatment. You will be informed if the study involves randomization.

During the trial, you will be closely monitored by our medical staff. If you experience any side effects, we will address them promptly. You will also have regular opportunities to discuss any concerns with the research team.

Study visits may include physical exams, lab tests, diagnostic procedures, and treatments related to the clinical trial. The frequency and length of visits will depend on the specific study, and we’ll provide you with a detailed schedule in advance.

The length of a clinical trial varies depending on the study. Some trials may last a few weeks or months, while others can span several years. We will inform you of the study duration during the consent process.