Characterisation of the Biochemical Profile and Physiology of the Coronary Circulation in Takotsubo Syndrome

Status: Recruiting
Location: See location...
Intervention Type: Diagnostic test
Study Type: Observational
SUMMARY

Consecutive consenting patients over the age of 18 years diagnosed with Takotsubo syndrome according to the position statement of the European Journal of Heart Failure (2016) will be included in the study. The primary endpoint is to evaluate the incidence of coronary microcirculation dysfunction and its correlation with the clinical presentation and the prognosis in patients with TAKO-Tsubo syndrome. Secondary endpoints will be to assess the incidence of in-hospital mortality, the prevalence of cardiogenic shock, the correlation between the levels of biomarkers analyzed, microvascular dysfunction, perceived quality of life, and angina severity during hospitalization and at subsequent follow-ups, and the influence of knowledge of the level of microvascular dysfunction on clinical management and prescribed therapies. Enrolment: 2 years, follow-up: 1 month and 1 year. Total: 3 years.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 90
Healthy Volunteers: f
View:

• Age ≥ 18 years;

• Diagnosis of Takotsubo syndrome

• Signing of informed consent

Locations
Other Locations
Italy
AOU Città della Salute e della Scienza
RECRUITING
Turin
Contact Information
Primary
Ovidio De Filippo, MD
odefilippo@cittadellasalute.to.it
+390116336023
Time Frame
Start Date: 2024-07-10
Estimated Completion Date: 2027-06-27
Participants
Target number of participants: 50
Sponsors
Leads: A.O.U. Città della Salute e della Scienza

This content was sourced from clinicaltrials.gov