DRKS00024889
Recruiting
Not Applicable
An observational clinical study to assess and assessment of the risk of bleeding after dentoalveolar procedures with Medication with direct oral anticoagulants (DOAKs), antiplatelet agents, and vitamin K antagonists. - DOAC
Mund-Kiefer- und Gesichtschirurgische KlinikFAU Uniklinik Erlangen0 sites300 target enrollmentMarch 29, 2021
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- D68.33
- Sponsor
- Mund-Kiefer- und Gesichtschirurgische KlinikFAU Uniklinik Erlangen
- Enrollment
- 300
- Status
- Recruiting
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Patient is taking DOACs (dabigatran, rivaroxaban, apixaban, or edoxaban), antiplatelet agent, vitamin K antagonist
- •\- Oral surgery procedures include implant placement, tooth extraction, Flapoplasties, osteotomies (more specifically, up to 3 implants and 3 teeth per jaw, osteotomies of teeth (including wisdom teeth), augmentations limited to sinus lift in the upper jaw with one or two implants)
Exclusion Criteria
- •the oral surgery is performed under intubation anesthesia and/or inpatient admission is inpatient admission is necessary preoperatively
- •\- Patient with congenital hemorrhagic diathesis
- •\- Larger augmentations (bone block chin or jaw angle) or if a second second surgical area is necessary for this
- •\- Patients with co\-morbidities that preclude local and ambulatory treatment
- •exclude local and outpatient treatment, the risk of bleeding is assessed as increased
Outcomes
Primary Outcomes
Not specified
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