Low Cardiac Output Syndrome Clinical Trial
Official title:
Cardiovascular Events in Patients With Low Cardiac Output Undergoing Local Dental Anesthesia With and Without Epinephrine: Randomized, Double-blind Pilot Study
Verified date | April 2024 |
Source | University of Sao Paulo General Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Patients with low cardiac output syndrome requiring surgical and periodontal dental treatment will be selected to undergo the dental procedure using local dental anesthetic: 2% lidocaine with epinephrine and 2% lidocaine without vasoconstrictor. Cardiovascular events and the safety of using two cartridges (3.6 mL) will be evaluated. They will be evaluated by Holter monitoring in the period of 1 hour before, during and 1 hour after the procedure and blood pressure correction will be performed
Status | Recruiting |
Enrollment | 29 |
Est. completion date | December 1, 2024 |
Est. primary completion date | December 1, 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Patients with advanced heart failure, in INTERMACS III using dobutamine at 5 to 20 µg/kg/minute due to low cardiac output syndrome - Presence of periodontal disease, in the 4th or 6th sextant with indication of supragingival and/or subgingival periodontal scaling; - Residual root or teeth with periodontal disease in the jaw, with simple extraction indicated. Exclusion Criteria: - Patients with a ventricular assist device such as an intra-aortic balloon implanted less than 24 hours after the dental procedure or with extracorporeal membrane oxygenation (ECMO); - Using other inotropes; - On mechanical ventilation; - Continuously using a non-invasive ventilation mask; - In septic shock; - Presence of acute myocardial infarction <30 days; - Patients with terminal non-cardiac disease, cyanotic congenital heart disease or cardiomyopathies with arrhythmogenic potential (arrhythmogenic dysplasia, hypertrophic cardiomyopathy, non-compacted myocardium); - Pregnant women; - History of sudden death recovered < 1 month ago; - In the recent postoperative period of cardiac surgery (5 days); - Allergic to sodium bisulfite and methylparaben, preservatives of epinephrine and the anesthetic cartridge, respectively. |
Country | Name | City | State |
---|---|---|---|
Brazil | Instituto do Coração HCFMUSP | São Paulo |
Lead Sponsor | Collaborator |
---|---|
University of Sao Paulo General Hospital | Coordenação de Aperfeiçoamento de Pessoal de Nível Superior. |
Brazil,
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* Note: There are 15 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Amount ventricular and supraventricular arrhythmia | Number of ventricular and supraventricular arrhythmias recorded using Holter | during dental procedures |
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