Polish Registry of Takotsubo Syndrome
ConditionTakotsubo Syndrome
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorMedical University of Warsaw
About this trial
Polish registry of takotsubo syndrome
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
None
Disqualifiers
None
Trial population
Patients hospitalised with takotsubo syndrome in Poland
Trial design
Design model
Cohort
Time perspective
Other
Treatments tested in this trial
No intervention
Other interventionNo intervention
Treatment groups
No treatment groups listed
Trial outcomes
Primary outcomes
1
Number of participants with in-hospital complications and mortality
In hospital complications include atrial fibrillation, ventricular tachycardia, ventricular fibrillation, atrioventricular block, cardiogenic shock, cardiac arrest
Time frame
through study completion, an average of 1 yearSecondary outcomes
1
Number of participants with complications with echocardiography
Complications include: severe mitral regurgitation, fluid in the pericardium, right ventricle disfunction, ventricular septum rupture
Time frame
through study completion, an average of 1 yearSponsors and contacts
Click on the lead sponsor to view all of their trials.
Source ClinicalTrials.gov