Coronary disease
Conditions
Interventions
This is a prospective, randomized, controlled, single center, non blinded clinical study. Study subjects will be evaluated for standard clinical parameters, coronary risk factors, demographic data, an
Sponsors
Associação Paranaense de Cultura
Associação Paranaense de Cultura
Eligibility
Inclusion criteria
Inclusion criteria: Patients between 18-75 years who have favorable criteria post-intervention, including a Thrombolysis In Myocardial Infarction (TIMI) of 3 in the blood vessel. Absence of occlusion on relevant lateral branches with diameter of = 2 mm. Absence of coronary dissections
Exclusion criteria
Exclusion criteria: ST-segment elevation myocardial infarction (STEMI). Cardiogenic shock. Total obstruction of the targeted blood vessel. Need for left coronary branch or emergency intervention due to persistent chest pain. Clinical instability associated with the reduction of coronary blood flow (TIMI<3). Major bleeding (BARC>1). Prohibition of radial artery access. Need for prolonged anticoagulant therapy. Persistent chest pain. Alterations on the electrocardiogram suggestive of ischemia on the observation period (6 hours after the procedure). Pregnancy. Active malignancies. Simultaneous participation on other clinical trials. Absence of adequate family support
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to find that same day discharge will be equally safe and non inferior when compared to regular discharge proceedings with overnight stay | — |
Secondary
| Measure | Time frame |
|---|---|
| It is expected to find that patients who undergo same day discharge will be more satisfied with the treatment, when compared to the ones who stayed overnight | — |
Countries
Brazil
Contacts
Public ContactRomulo Torres
Pontifícia Universidade Católica do Paraná
Outcome results
None listed