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临床试验/TCTR20200402006
TCTR20200402006招募中2 期

Comparative Study of Efficacy and Safety of M-Bone (Biphasic Calcium Phosphate with Hydroxyapatite:Beta-tricalcium Phosphate of 70:30) versus Reference Commercial Product for Socket Preservation

Assistive Technology and Medical Devices Research Center (A-MED)0 个研究点目标入组 48 人开始时间: 2020年4月2日最近更新:
适应症

试验速览

阶段
2 期
状态
招募中
发起方
入组人数
48

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
20 Years 至 80 Years(—)
性别
All

入选标准

  • 1. Subjects must be above 20 years of age and generally healthy.
  • 2. Subjects who can tolerate local anesthetic injection
  • 3. Subjects who are going to undergo extraction and subsequent implant placement due to periodontal disease, endodontic failure, advanced unrestorable caries, or tooth fracture. The indicated tooth should be bounded by adjacent teeth.
  • 4. Subjects who agree to refrain from using medication that affect wound healing such as anti-angiogenic/anti-resorptive drugs after operation
  • 5. Subjects who agree to refrain from using nonsteroidal anti-inflammatory drugs (NSAIDs) and antibiotics within 14 days after operation on Day 1 except that prescribed by investigator after operation.
  • 6. Subjects who have the ability to understand the requirement of the study and must voluntarily sign and date an inform consent. If subjects are unable to read or may not fully understand the requirement of the study, such as elderly subjects, subject's legally acceptable representative (such as relatives), as witness should sign and date an inform consent.

排除标准

  • 1.Subjects who are known hypersensitivity to local anesthetic agents
  • 2.Subjects with metabolic bone disease or any disease (from investigator's opinion) that may increase risk of subjects. This includes but not limit to uncontrolled hypertension, uncontrolled diabetic mellitus, severe hepatic impairment or end-stage renal failure.
  • 3.Pregnancy or lactation subjects (by interviewing).
  • 4.Subjects who have history of malignancy or radiotherapy or chemotherapy for malignancy in the past 5 years.
  • 5.Subjects who have history of autoimmune disease, have long-term use of steroids or antibiotics, have any sign of any active infection or have any disease that in investigator's opinion has affect on the healing of wound.
  • 6.Subjects with alcohol abuse or excessive use or alcoholism (in the opinion of the investigator, as judged by medical history)
  • 7.Subjects who smoke more than 10 cigarettes per day
  • 8.Subjects who are not able to follow instructions related to the study procedures.
  • 9.Subjects who take anti-coagulant medication.

研究者

发起方
Assistive Technology and Medical Devices Research Center (A-MED)

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