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NCT02141750 Clinical Trial

THIRD NATIONAL REGISTRY OF ACUTE CORONARY SYNDROMES

Acute Coronary Syndromes Clinical Trial

— RENASICA_III  

Official title:
THIRD NATIONAL REGISTRY OF ACUTE CORONARY SYNDROMES

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02141750
Other study ID # RENASICA III
Secondary ID
Status Completed
Phase N/A
First received May 15, 2014
Last updated May 15, 2014
Start date November 2012
Est. completion date November 2013

Study information
Verified date May 2014
Source Third National Registry of Acute Coronary Syndromes
Contact n/a
Is FDA regulated No
Health authority Mexico: Mexican Society of Cardiology
Study type Observational

Clinical Trial Summary

The Registry pretends to identify stratification, diagnosis and treatment approaches in patients with Acute Coronary Syndrome (ACS) in community hospitals with tertiary hospitals to optimize resources and identify strategies to improve health care quality through the creation of clinical guidelines that serve for unify management and treatment methods with adherence to international guidelines which include suggestions for treatment and medication.

Recruitment information / eligibility
Status Completed
Enrollment 8296
Est. completion date November 2013
Est. primary completion date July 2013
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

all patients with suspected ACS and will analyze risk factors, chest pain and electrocardiographic characteristics.

Exclusion Criteria:

Patients with secondary ischemia (anaemia, pulmonary thromboembolism, myocarditis) and type II infarction.

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Third National Registry of Acute Coronary Syndromes

Outcome
Type Measure Description Time frame Safety issue
Primary Number of patients with complications after presenting ACS The main objective will be to know the evolution of ACS in third and second level hospitals with a monitoring at a minimum of one year for each patient. up to one year No
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