Evaluation of postoperative bleeding of oral surgeries in patients taking oral anticoagulants.
Not Applicable
Recruiting
- Conditions
- heart disease, oral bleeding, anticoagulantsC14.280C07.465.625
- Registration Number
- RBR-83qw93
- Lead Sponsor
- niversidade Federal de Sergipe
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- Not specified
Inclusion Criteria
Patients taking oral anticoagulants for at least 14 days; patients with indication of small oral surgeries; patients with INR (International Normalized Norm) between 1.5 and 4.0 the day before the procedure.
Exclusion Criteria
Patients with blood dyscrasia or other conditions that alter blood clotting; patients smokers; diabetic patients; pregnant or lactating patients; patients with a history of allergy to tranexamic acid or reabsorbable collagen gelatin; patients using medications that may interact with medications used in this study; oral surgeries that last 40 minutes; oral surgeries with large osteotomies (third molars included and impacted); patients with INR above 3.5
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method