Applicability of Syncope Guidelines in Cataluña

NCT ID: NCT01721369

Last Updated: 2025-07-02

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

View full results

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

581 participants

Study Classification

OBSERVATIONAL

Study Start Date

2011-11-30

Study Completion Date

2013-03-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

The aim of SYNCAT study is to analyze the level of adherence of Syncope Guidelines ESC2009 for the management, diagnosis and treatment of syncope in a specific territory with similar health structure, the region of Cataluña in Spain that includes aprox. 7,000,000 inhabitants, including different complexity level of hospitals and the impact that following guidelines can have in the prognosis of these patients.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Brief Loss of Consciousness

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Transient Loss of Consciousness (T-LOC)

Transient Loss of Consciousness (T-LOC). Treatment according to normal clinical practice.

Transient Loss of Consciousness (T-LOC)

Intervention Type DIAGNOSTIC_TEST

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Transient Loss of Consciousness (T-LOC)

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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
Minimum Eligible Age

15 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Medtronic Cardiac Rhythm and Heart Failure

INDUSTRY

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Angel Moya, Dr.

Role: PRINCIPAL_INVESTIGATOR

Hospital Vall d'Hebron

Jordi Tomàs, Dr.

Role: PRINCIPAL_INVESTIGATOR

H. Arnau de Vilanova de Lleida

Joan Nicolàs, Dr.

Role: PRINCIPAL_INVESTIGATOR

Parc Sanitari Sant Joan de Déu

Jordi Mercè, Dr.

Role: PRINCIPAL_INVESTIGATOR

H. Joan XXIII

Francesc Planas, Dr.

Role: PRINCIPAL_INVESTIGATOR

H. Municipal de Badalona

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

SYNCAT

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

CSRS Implementation - A Pilot Study
NCT04790058 ACTIVE_NOT_RECRUITING