Skip to content

Registry Of Acute meDical Emergencies in Brazil

Registry Of Acute meDical Emergencies in Brazil - ROAD-Brazil

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02753023
Acronym
ROAD-Brazil
Enrollment
1650
Registered
2016-04-27
Start date
2015-05-31
Completion date
2020-05-31
Last updated
2018-10-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Coronary Syndromes, Aortic Aneurysm, Familial Thoracic 1, Chest Pain, Heart Failure, Pulmonary Edema, Pulmonary Embolism, Syncope

Brief summary

Critical patients in emergency room are seriously situations that need quickly diagnosis and treatment. Different predictors of prognosis can be related with mortality and morbidity in-hospital and in long-term. In Brazil, this kind of registry is not available. The aim of the study is analysis and report data about critical patients in Emergency Departments over all country, showing demographic, clinical and prognosis data about that in Brazil.

Detailed description

This will be a prospective and multicentric data-bank registry. Initially, all patients with acute coronary syndromes (ACS), acute decompensated heart failure (ADHF), warfarin intoxication, acute pulmonary edema, acute aortic dissection, chest pain, pulmonary embolism and syncope will be included. There will be not exclusion criteria. The inclusion criteria will be followed by definition of each illness described in recent guidelines. Investigators estimated annually over than 500 cases with ACS/chest pain, 300 cases of ADHF, 200 cases of aortic dissection, 200 of pulmonary embolism, 200 cases of warfarin intoxication, 100 cases of syncope and 150 of acute pulmonary edema. Clinical data, electrocardiographic and echocardiographic findings, laboratory results and prognosis will be related. Routine of treatment will be defined by each center. The analysis includes minimum, medium and maximum values. Variables will be adjusted according with each diagnosis and all data will be included using the REDCap digital data entry. Probabilities will be determined by logistic regression and will be considered significate when p \< 0.005. Prospectively, investigators will use the Cox model to calculate associations.

Interventions

OTHERno intervention

No intervention related

Sponsors

University of Sao Paulo General Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

* all patients with: * acute coronary syndromes (ACS) or, * acute decompensated heart failure (ADHF) or, * warfarin intoxication or, * acute pulmonary edema or, * acute aortic dissection or, * chest pain or, * pulmonary embolism or * syncope.

Exclusion criteria

-There will be not

Design outcomes

Primary

MeasureTime frame
mortality6 months

Secondary

MeasureTime frame
mortality12 months

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026