Our approach

You will receive a comprehensive informed consent procedure, during which the study objectives, protocol, and potential risks and benefits are clearly explained. We will carefully assess whether you meet the eligibility criteria, always with full respect for your privacy and personal data. You will have ample time to consider your participation, raise any questions, and consult with your loved ones or treating physician if you wish.

You decide entirely voluntarily whether you wish to participate. Prior to providing written informed consent, we ensure that all information is fully understood and that every question is answered thoroughly.

We coordinate all necessary pre-study procedures, including scheduled appointments, clinical assessments, and any required study medication, in preparation for your participation.

Throughout the study, you will be closely monitored and guided by our qualified physicians and study leads. Patient safety, comfort, and transparent communication remain our highest priorities at every stage of the process.

Following the active study period, structured follow-up visits and clinical evaluations are conducted to monitor your health and ensure your wellbeing, while gathering the necessary research data to contribute to the overall study outcomes.

Where possible, the outcomes of the research are communicated to you in a clear and transparent manner. Personalised medical advice and support are provided where relevant to your individual health situation.