A clinical trial is a scientific study conducted to evaluate the safety and effectiveness of new drugs, treatments, or medical devices. These studies are carried out on volunteer participants and aim to improve healthcare services.
Clinical trials are essential to ensure that new treatments are safe and effective. Through these studies, new methods for preventing, diagnosing, and treating diseases can be developed.
Each clinical trial has its own specific eligibility criteria. Some trials seek healthy volunteers, while others target individuals with specific medical conditions. The criteria vary depending on the study’s purpose and type.
As with any medical intervention, there may be some risks in clinical trials. These risks can range from side effects to temporary changes in quality of life. All potential risks are thoroughly explained to participants.
Participants may have access to new treatments that are not yet available on the market. They also contribute to medical science and the treatment of future patients. In some cases, participants may receive closer medical monitoring and free healthcare services.
All clinical trials are subject to strict rules and regulations to ensure the safety of participants. In Turkey, they are monitored by the TİTCK and ethics committees. Furthermore, they are conducted in accordance with international standards, such as Good Clinical Practice (GCP) guidelines.
No, participation in clinical trials is free of charge. In some cases, participants may even be compensated for transportation or other expenses.
Yes, you can withdraw from a clinical trial at any time, for any reason, without providing an explanation. This will not affect the healthcare services you receive.
Your personal and medical information is kept confidential under legal regulations and ethical guidelines. The data is typically anonymized and used solely for research purposes.
Yes, before participating, you will be provided with detailed information about the study’s purpose, duration, procedures, possible risks, and benefits through the “Informed Consent Form.” All your questions will be answered, and you will be given time to consider your decision.
Yes, in most cases, you can continue seeing your regular doctor. However, there may be restrictions required by the research protocol in some cases. You will be informed of these in advance.
Yes, most research centers provide general information about the results to participants after the study is completed. However, it may take some time to prepare this information.
Yes, under Turkish regulations, all clinical trial volunteers must be insured. This insurance, provided by the study sponsor, is completely free for you and covers any harm or disability that may arise due to the trial. The insurance coverage includes the period from the start to the end of the study and often extends for a specified time after the study is completed. The details of the insurance are explained in the “Informed Consent Form,” and the research team will provide you with comprehensive information.
For more information, please do not hesitate to contact our research team.