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临床试验/DRKS00024889
DRKS00024889招募中不适用

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 个研究点目标入组 300 人开始时间: 2021年3月29日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
300

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 Years 至 one(—)
性别
All

入选标准

  • 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)

排除标准

  • 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

研究者

发起方
Mund-Kiefer- und Gesichtschirurgische KlinikFAU Uniklinik Erlangen

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