EUCTR2019-000902-31-ES进行中（未招募）1 期
Healing efficacy after impacted mandibular third molar surgery with the use of autologous platelet-rich fibrin: a randomized controlled clinical study
OMEQUI0 个研究点目标入组 36 人开始时间: 2019年7月5日最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 36
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
入选标准
- •Patients> 18 years.
- •Presence of oral health (periodontally healthy or with treated periodontitis), with a BoP <20% and a PI <20%.
- •Systemically healthy, without any disease that may contraindicate minor oral surgery, that does not take any medication that may influence coagulation and / or that takes any NSAID or paracetamol daily.
- •Non-smokers or smokers of <10 cigarettes/day.
- •No pregnancy or lactation.
- •The tooth to be extracted will be included or semi-included and will have fully formed roots.
- •Absence of infectious and cystic pathology in the molar to be extracted.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 36
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Patients who due to systemic conditions are not possible to draw blood.
- •Penicillin allergy.
- •Allergy to ibuprofen and / or paracetamol.
- •Diseases that limit the use of ibuprofen and / or paracetamol.
研究者
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