Oral Surgical Procedures
Conditions
Interventions
This is a randomized clinical trial with 2 arms, based on the CONSORT protocol. The researcher responsible for randomization will not have access to the recruitment of individuals and the researcher w
G09.188.390
Sponsors
Universidade de Cuiabá
Hospital Geral e Maternidade de Cuiabá
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Volunteers using anticoagulant therapy continuously; with Surgical indication for tooth extraction; with international normalized ratio (INR) values reported by prothrombin time of up to 3.5; who agree to participate in the research and sign the term of free and informed consent (TCLE) specific to the research in question
Exclusion criteria
Exclusion criteria: Volunteers with changes in preoperative laboratory tests that contraindicate dental surgery; when, for any reason, they suspend the continuous use of medication prior to surgery; individuals who do not cooperate with the postoperative instructions that interfere with the maintenance of the clot
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| It is expected to find the presence of mediate postoperative bleeding (yes or no), from the 2nd to the 7th postoperative day | — |
Primary
| Measure | Time frame |
|---|---|
| Hemostasis is expected in the immediate postoperative period, in the first 24 hours after surgery. | — |
Countries
Brazil
Contacts
Public ContactAlexandre Borba
Hospital Geral e Maternidade de Cuiabá
Outcome results
None listed