Brief Loss of Consciousness Clinical Trial
— SYNCATOfficial title:
Observational Study of the Application of the ESC2009 Syncope Guidelines in Cataluña
NCT number | NCT01721369 |
Other study ID # | SYNCAT |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | November 2011 |
Est. completion date | March 2013 |
Verified date | September 2020 |
Source | Medtronic Bakken Research Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The aim of SYNCAT study is to study the level of adherence of the centers in Cataluña tu the Syncope Guidelines ESC2009 for the diagnosis and treatment of syncope and the impact that following them can have in the prognosis of these patients.
Status | Completed |
Enrollment | 581 |
Est. completion date | March 2013 |
Est. primary completion date | March 2013 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 15 Years and older |
Eligibility |
Inclusion Criteria: - Each patient that comes from the Emergency room and/or in office doctors visit (Internal Medicine, Cardiology, Neurology...) with Transient Loss of Conscience (T-LOC) Exclusion Criteria: - Patients younger than 15 years old - Pregnant women |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Medtronic Bakken Research Center |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Number of Patients That Adhere to the 2009 Syncope Guidelines (ESC2009) | To analyze the number of patients that an etiologic diagnose was established according to the New Syncope Guidelines ESC2009 in the hospital care, in a particular community with hospitals with different levels of care in a specific region of Spain. | 12 months |