FAQ

  • Eligibility criteria vary widely depending on the specific trial. Factors may include age, gender, type and stage of disease, previous treatment history, and other medical conditions. Our team conducts a thorough screening process to determine eligibility for each study.

  • The duration varies significantly based on the type of trial. Some may last a few weeks, while others can continue for several years. During the informed consent process, you'll be provided with the expected timeline for your specific trial, including the frequency of visits and total duration.

  • Your safety is our top priority. You'll be given contact information for the research team to report any side effects immediately. The team will assess the situation, provide appropriate medical care, and determine if adjustments to your participation are needed. All potential known side effects are discussed during the informed consent process.

  • Yes, participation is always voluntary. You can withdraw from a study at any time and for any reason. If you decide to leave, we may ask you to come in for a final visit to ensure your safety and well-being. Withdrawing from a trial will not affect your access to other medical care.

  • Many trials provide compensation for time, travel, and inconvenience, though the amounts vary. Compensation details are always discussed during the informed consent process. It's important to note that any compensation is for your time and effort, not for accepting risk.

  • Yes, we adhere to strict privacy protocols. Your personal information and medical data are protected according to federal regulations. While the results of trials are published, individual participants are never identified without explicit permission.

Common Questions

Learn more about participating in clinical trials

Participation offers several benefits: access to promising new treatments before they're widely available, expert medical care, and the opportunity to contribute to medical science. Your involvement helps researchers develop better treatments for future patients.

All clinical trials follow strict protocols reviewed by ethics committees. Before starting, you'll go through an informed consent process explaining all aspects of the trial. Throughout the study, researchers monitor participants closely, and you can withdraw at any time.

Yes, we encourage you to continue your relationship with your primary healthcare provider. We'll coordinate with them regarding your participation and share relevant information with your permission.

Most clinical trials cover the costs of research-related medical care and the study medication. Some trials also provide compensation for time and travel expenses. Your specific coverage would be outlined in detail before you enroll.

After signing up, our team will contact you to discuss your eligibility. If you meet the initial criteria, you'll be invited for a screening visit where we'll conduct a thorough health assessment. If eligible, we'll explain the trial in detail before you decide whether to participate.

You have the right to withdraw from a trial at any time for any reason. If you decide to leave, we'll ask about your reasons and may request a final follow-up visit to ensure your safety and well-being.