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OpenTrials
Completed

NCT Number: NCT00958958

Brazilian Intervention to Increase Evidence Usage in Practice - Acute Coronary Syndromes

Phase 1: An observational study (registry) will be conducted which will objectively document the ACS clinical practice in Brazilian public hospitals, and identify the important barriers for the evidence usage incorporation in the clinical practice.

Phase 2: A Cluster randomized clinical trial in which public hospital will be randomized to receive or not a multifaceted strategy in order to increase evidence based therapy in clinical practice.

Completed

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Hospital do Coração

São Paulo, 04005-000, Brazil

About this study

STUDY POPULATION:

Patients with thoracic pain who the emergency department physician suspects of ACS and plans start a treatment for this issue; It will be excluded patients transferred of others institutions with 12 hours of symptoms.

PROGRAM:

There are multifaceted Interventions Including

  • Distribution of educational materials
  • Case manager: Use of a trained person who works in the hospital and will be responsible to assure that all interventions were used
  • Reminders: specific information that is designed or intended to prompt a health professional to recall information (patient bracelets, labels, posters, pocket cards, checklists).
  • Practical training

ENDPOINTS:

Phase 1 Primary outcome; patient who've received interventions based on evidence proportion informed by the indicators; Phase 2

Primary outcome:

Increase of prescription of evidence based treatment in clinical practice Secondary outcome Total mortality and major cardiovascular events

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Patient Eligibility criteria

Inclusion criteria

  • Patients with thoracic pain who the emergency department physician suspects of ACS and plans start a treatment for this issue

Exclusion criteria

  • Patients transferred from others institutions within 12 hours of the symptoms

Cluster Eligibility Criteria

  • National Public Hospitals with emergency department. A cluster can be one hospital with emergency department, or 2 or more hospitals (for example: 1 emergency hospital and 1 general hospital which receive the patients to perform PCI).

Treatment and study plan

multifaceted strategy

Other

There are multifaceted Interventions Including

  • Distribution of educational materials: distribution of published or printed recommendations for clinical care.
  • Case manager: Use of a trained person who works in the hospital and will be responsible to assure that all interventions were used
  • Reminders
  • Practical training

Primary outcomes

  1. Phase 1: patient who've received interventions based on evidence proportion informed by the indicators

    Time frame: 9 months

  2. Phase 2: increase of prescription of evidence based treatment in clinical practice

    Time frame: 6 months

Secondary outcomes

  1. Total mortality and major cardiovascular events

    Time frame: 6 months

Sponsors and collaborators

Lead sponsor

Hospital do Coracao

Other

Collaborators

  • Ministry of Health, Brazil

Registry information

Acronym: BRIDGE

Important dates

Study start
2010
Primary completion
2012
Study completion
2012
First posted
Aug 14, 2009
Registry last updated
Feb 28, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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