EUCTR2013-003323-11-IT进行中（未招募）1 期
RANDOMIZED CLINICAL TRIAL, PLACEBO-CONTROLLED, SPLIT-MOUTH, ADOUBLE-BLIND, FOR THE EVALUATION OF THE EFFECTIVENESS OF PREemptiveANALGESIA BY ADMINISTRATION OF IBUPROFEN 400MG, FOR THECONTROL OF POSTOPERATIVE ACUTE PAIN in the extraction of IMPACTEDTHIRD MOLAR MANDIBULAR - PRE-EMPTIVE ANALGESIA
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 入组人数
- 21
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
- 性别
- All
入选标准
- •males and females aged between 18 and 40 years, absence of systemic
- •disease (ASA class I), non-smoking or smoking <10 cigarettes / day;
- •plaque index and bleeding less than 25%, indicating to extract both
- •lower wisdom teeth inclusion in partial or total bilateral bone
- •(osteotomy applicant), similar in depth, inclination and position, no
- •medication in the 10 days prior to the extraction, presence in the arch of
- •the first and second molars, absence of pain and associated osteolytic
- •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 21
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Exclusion criteria will be: persons under age or older than 40 years old; subjects with systemic diseases; Smoking <10 cigarettes / day; plaque index and bleeding than 25%; individuals with anatomical differences between the lower wisdom teeth inclusion in partial or total bilateral bone (osteotomy applicant), with respect to the depth, the 'tilt and position; subjects who took drugs in the 10 days prior to extraction; absence in the arch of the first and second molar; the presence of lytic bone disease and pain symptoms associated with items to be extracted.
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