Do I pay for participation?
No. Study-related procedures, diagnostics and treatment are covered within the clinical trial protocol.
Promente Clinical Research Center
Clinical trials for patients
Check current recruitment and learn how participation in a clinical trial works.
Recruiting
Neumora NMRA-335140-303
Clinical trial of an investigational molecule for patients with depression.
Learn moreRecruitingJANSSEN 42847922MDD3003
Clinical trial for patients with depression and sleep-related symptoms.
Learn moreRecruitingEMBRACE CYB003-003
Study of an investigational psychedelic substance with psychological support in depression.
Learn moreOngoingCOMP 006 - COMP360 psilocybin therapy research
Clinical research for adults with treatment-resistant depression.
Learn moreWho can participate?
Each clinical trial has specific inclusion and exclusion criteria. Participation is possible after medical assessment, protocol review and informed consent.
Study-related procedures are free of charge for participants. When the protocol allows it, travel or accommodation costs may be covered or reimbursed.
Clinical research coordinators
People interested in participation can contact the site reception or the clinical research coordinator.
- Registration: 790 219 220, kontakt@pro-mente.pl
- Malgorzata Megger: 790 219 231, m.megger@pro-mente.pl
Frequently asked questions
Can I withdraw?
Yes. Participants may withdraw according to the informed consent process without losing their right to regular medical care.
What is placebo?
Placebo is an inactive comparator used in some studies. The protocol explains whether placebo may be used and how randomization works.