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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.

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

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00024889
Enrollment
300
Registered
2021-03-29
Start date
2019-04-03
Completion date
Unknown
Last updated
2025-10-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

A01 Z92.1 A01

Interventions

Group 1: Extraction of tooth

Sponsors

Mund-Kiefer- und Gesichtschirurgische KlinikFAU Uniklinik Erlangen
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion 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

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

Design outcomes

Primary

MeasureTime frame
Postoperative Bleeding risk as a function of anticoagulation and surgical Intervention within the first 10 days postoperatively

Secondary

MeasureTime frame
Derivation of risk stratification for anticoagulated patients and postoperative rebleeding.

Countries

Germany

Contacts

Public ContactMayte Buchbender

Mund-Kiefer- und GesichtschiurgieZMK Klinik, FAU Erlangen

mayte.buchbender@uk-erlangen.de09131-8533614

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 21, 2026