EUCTR2008-003946-28-IT进行中（未招募）不适用
Postoperative pain treatment following gynecologic surgery, using different doses of transdermal buprenorphine a double ? blind, randomized study - Transdermal buprenorphine for the treatment of postoperative pain
ISTITUTO PER L`INFANZIA BURLO GAROFOLO0 个研究点开始时间: 2009年3月10日最近更新:
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
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
- Female
入选标准
- •-Patients elective for laparotomic hysterectomy; -Age from 35 to 60 years; -Patients ASA I/II; -Patients can provide a written informed consent.
- •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
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •-Patients with age >35 and <60 years; -Patients with severe liver inssuficiency; -Patients with obesity (BMI> 27); -Patients with known hypersensitivity to buprenorphine or any other ingredients; -Patients addicted to opioids and in treatment of abstinence from drugs; -Patients with diseases in which the respiratory apparatus and respiratory function are severely compromised; -Patients who take or have taken MAO inhibitors in the last two weeks; -Patients who take opioids, antidepressants, hypnotics and/or NSAIDs; -Patients with psychiatric disorders; -Patients not cooperating and/or with psychological disorders
研究者
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