RUDRA Registry (Real-World Clinical Registry for Patients With Recurrent Pericarditis) (NCT06517966) | Clinical Trial Compass
Active — Not RecruitingNot Applicable
RUDRA Registry (Real-World Clinical Registry for Patients With Recurrent Pericarditis)
Russia100 participantsStarted 2024-09-30
Plain-language summary
А multicenter, non-interventional real world clinical registry of patients with recurrent pericarditis.
The main goal of the registry is to epidemiologically assess the pattern, clinical outcomes, and approaches to therapy in patients with recurrent pericarditis.
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion criteria
. Men or women 18 years of age or older at the time of data recording or pericarditis debut;
. Presence of one of the following conditions:
Exclusion criteria
. Age below 18 years at the time of inclusion in the registry or debut of pericarditis;
. Specialist-confirmed secondary genesis of RP (infectious, autoimmune, neoplastic, metabolic, traumatic, iatrogenic, etc.); 2. Manifestations and complications of myocarditis, various diseases of thoracic organs, systemic diseases, cardiac surgery, radiation therapy, tuberculosis, etc.);
. lack of possibility of screening examination and dynamic follow-up;
. Organ/tissue transplantation less than 5 years prior to study inclusion or debut of pericarditis;
. Oncologic disease less than 3 years prior to study inclusion or pericarditis debut;
. Chemotherapy with anthracycline-type drugs at the time of pericarditis debut;
. Administration of amphetamine-type drugs at the time of pericarditis debut;
. Cardiac/pericardial surgery in the last 6 months prior to study inclusion or pericarditis debut;
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.