We are updating the design of this site. Learn more.
Show more
ClinicalTrials.gov Menu

Syncope in Cataluña SYNCAT (SYNCAT)

This study has been completed.
ClinicalTrials.gov Identifier:
First Posted: November 5, 2012
Last Update Posted: April 9, 2014
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Medtronic Bakken Research Center
The SYNCAT study intention 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.

Brief Loss of Consciousness

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Observational Study of the Application of the ESC2009 Syncope Guidelines in Cataluña

Resource links provided by NLM:

Further study details as provided by Medtronic Bakken Research Center:

Primary Outcome Measures:
  • Correct application of Guidelines [ Time Frame: 1 year follow up ]
    Percentage of patients in which the guidelines have been correctly applied for the evaluation of syncope

Enrollment: 581
Study Start Date: November 2011
Study Completion Date: March 2013
Primary Completion Date: March 2013 (Final data collection date for primary outcome measure)

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

Ages Eligible for Study:   15 Years and older   (Child, Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
Patients with Transient Loss of Conscience: T-LOC

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
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01721369

Sponsors and Collaborators
Medtronic Bakken Research Center
Principal Investigator: Angel Moya, Dr. Hospital Vall d'Hebron
Principal Investigator: Jordi Tomàs, Dr. H. Arnau de Vilanova de Lleida
Principal Investigator: Joan Nicolàs, Dr. Parc Sanitari Sant Joan de Déu
Principal Investigator: Jordi Mercè, Dr. H. Joan XXIII
Principal Investigator: Francesc Planas, Dr. H. Municipal de Badalona
  More Information

Responsible Party: Medtronic Bakken Research Center
ClinicalTrials.gov Identifier: NCT01721369     History of Changes
Other Study ID Numbers: SYNCAT
First Submitted: June 19, 2012
First Posted: November 5, 2012
Last Update Posted: April 9, 2014
Last Verified: April 2014

Additional relevant MeSH terms:
Consciousness Disorders
Neurobehavioral Manifestations
Neurologic Manifestations
Nervous System Diseases
Signs and Symptoms