Information for patients

Patient information

Contact to the research coordinator:
phone: 797 206 606
badaniakliniczne@medinet.pl

We invite you to take part in clinical trials concerning:

• cardiac surgery for adults and children
• cardiology
  
• anesthesiology and intensive care
  
• vascular surgery
  
• physiotherapy
• psychology

1. Participation in the study is completely free for the Patient. The patient has the right to complete protection of his personal data, to anonymity and to information about his health throughout the duration of the study.
2. Each clinical trial is conducted with the participation of qualified, trained and experienced medical personnel. This is verified by the Bioethics Committee by presenting the necessary documents (certificates, trainings, courses).
3. Before starting and entering the study, the Patient receives full information about the study, both in written and oral form - from the attending physician (researcher), and also signs a document of informed consent.
4. Participation in the study is completely voluntary. The patient may resign from the study at any time, retaining the full right to standard treatment and not suffering any consequences.
5. The studies are conducted according to the principles of Good Clinical Practice (GCP). It is an international standard for the principles of conducting clinical trials.
6. All clinical trials conducted at the Lower Silesian Center for Heart Diseases Medinet Sp. z o. o. in Wrocław are started after obtaining the consent of the President of the Office for Registration of Medicinal Products and Biocidal Products, as well as a positive opinion of the Bioethics Committee.