Yes, every clinical trial is strictly supervised by qualified medical professionals and independent ethics committees. Your health will be regularly monitored throughout the study to ensure the highest level of safety.
Participation in a clinical trial is only possible if a patient meets specific medical criteria defined in the study protocol. These typically include age, type of condition, overall health status, previous treatments, and laboratory test results.
During the screening visits, the physician and the research team will take your medical history, perform the necessary examinations, and assess whether participation is both safe and in line with the study requirements.
If you are not eligible for a specific study, the team may suggest other clinical trials or alternative treatment options available at the Centre.
The duration of a clinical trial depends on its type and phase. It may last a few weeks, several months, or even years. Detailed information about the study schedule will be provided during the screening process.
No, participation in a clinical trial is completely free of charge. You do not bear any costs for study visits, diagnostic tests, or treatment. All services provided within the study are funded by the sponsor.
If previous treatments have not brought the expected results, a new investigational medicine may help relieve your symptoms or support your current therapy. As part of the study, you will undergo a series of detailed diagnostic tests that are not typically performed in standard medical care.
Clinical trials are conducted both at our centre in Kraków (Centrum Nowoczesnych Terapii „Dobry Lekarz”) and at other specialised medical sites across Poland.
Some studies are carried out simultaneously in multiple countries, including Europe, the United States, and Asia.
The exact location depends on the specific study – during the screening process, patients are always informed where the treatment and follow-up visits will take place.
You can schedule a consultation by contacting us by phone or email - all contact details are available in the “Contact” section.
You can also use the convenient application form located below this FAQ section.
Once we receive your enquiry, our team will get in touch with you.
It depends on the phase of the clinical trial. Some medicines are already partially approved and are being further studied for new indications or dosages, while others are still in the pre-approval research stage.
During the screening visit, the physician will explain in detail the development stage of the investigational medicine and the rules for its use.
After the study is completed, the physician will discuss your results and propose further treatment options.
You may continue your care at our Centre or carry on treatment with your general practitioner or specialist. The decision on further treatment is made individually and always takes into account your safety and medical needs.
Yes. When you take part in a clinical trial, you are assigned a unique identification number that is used throughout all study documentation.
Your personal data is protected in accordance with applicable laws and data protection standards, including GDPR. Medical records are securely stored at our centre, and you have full access to your data and test results.
Our team is here to help. You can contact us by phone or email - all details are available in the “Contact” section.
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.
