Depending on whether a treatment method or a preventive intervention is being tested, either patients or healthy volunteers are recruited. They are, of course, subject to many criteria. Clinical trials comply with legal regulations, and participants sign informed consent to participate.
Registered volunteers are, of course, subject to multiple eligibility criteria. Clinical trials comply with legal regulations, and participants sign informed consent to take part.
During the visit, the physician or coordinator makes an initial assessment of whether the patient meets the basic eligibility criteria for participation in a clinical trial. The participant’s health condition, previous treatment, and the rules of participation in the study are discussed. The visit is informational in nature and does not obligate participation in the study.
This is a detailed eligibility assessment that includes medical examinations specified in the protocol. The patient receives full information about the study and signs informed consent. Based on the results, the physician decides whether to enroll the patient in the study.
After eligibility assessment, the patient is randomly assigned to one of the groups—receiving the investigational drug or placebo (or standard therapy). The process is controlled and ensures the reliability of the results. Typically, neither the patient nor the physician knows which group the participant has been assigned to.
The patient attends regular follow-up visits, receives the investigational medicinal product, and undergoes scheduled diagnostic tests. The medical team monitors the effectiveness of the therapy and the participant’s safety. Everything is conducted in accordance with the study protocol.
After completion of treatment, the patient remains under medical supervision to assess the long-term effects and safety of the therapy. Visits take place at scheduled intervals.
This is the final visit, during which the physician makes a final assessment of the patient’s participation in the study. The results and further medical recommendations are discussed, and participation in the project is formally concluded.
After receiving your application, we will contact you by phone. If we are currently conducting a clinical trial related to your condition, we will invite you for a consultation at our Centre.
During the appointment, our specialists will answer all your questions and discuss the available treatment options. Based on your health condition and the information provided, we will select the clinical trial that best meets your needs.
If we are not currently conducting a clinical trial suitable for you, we will keep your application and contact you when an opportunity arises to participate in a study tailored to your health condition.
