Cardiovascular diseases
Conditions
Interventions
Patients will be evaluated clinically by the researcher in the dental office of the InCor Dentistry Unit using a clinical mirror and explorer. Each patient should have two permanent upper and bilatera
Procedure/surgery
D27.505.954.502
E06.892
Sponsors
Faculdade de Odontologia da Universidade de São Paulo
Instituto do Coração do Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo
Faculdade de Medicina da Universidade de São Paulo
Eligibility
Age
18 Years to 85 Years
Inclusion criteria
Inclusion criteria: Volunteers who are being monitored at InCor / HCFMUSP; using oral anticoagulant (warfarin) only as the only medication capable of altering blood clotting and bleeding time; TP / INR (2.0-4.0), accepting to participate in the study; allow clinical examination; present bilateral upper permanent teeth with indication of extraction.
Exclusion criteria
Exclusion criteria: Patients with PT / INR outside the range defined by the study (2-4); patients using drugs such as antiplatelet agents in association with warfarin; with coagulopathies; with liver disease; with thrombocytopathies and thrombocytopenia; toothless upper patients; patients who do not have an indication for extraction; patients who do not accept to participate in the research for any reason.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Similar local hemostasis verified with the quantification of bleeding by means of gravimetry in mg in three moments: immediately after sutures, 72 hours and 8 days. | — |
Secondary
| Measure | Time frame |
|---|---|
| Best tissue repair, determined through the clinical repair scale at 72h and 8 days after suturing. | — |
Countries
Brazil
Contacts
Public ContactMariia;Sahar Naclério Hmomem;Ganz Riman
Faculdade de Odontologia da Universidade de São Paulo;Faculdade de Odontologia da Universidade de São Paulo
Outcome results
None listed