IRCT20131124015515N8已完成2 期
Efficacy and safety of Fentanyl Sublingual for treatment of Breakthrough Pain in Patients with Cancer
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 100
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
- 18 years 至 no limit（—）
- 性别
- All
入选标准
- •Age 18 and above
- •Patients with soft, visceral and bone marrow malignancies, patients with a diagnosis of malignant tumors or malignant tumors
- •At least 1-4 episodes of pain per day
- •Receiving an opioid regimen for the control of pain at a constant and similar dose (oral morphine or opioid similar to 60-1000 mg / day / oral oxycodone 30 mg daily)
- •Having informed consent to participate in the study
排除标准
- •History of receiving interatcal opioids
- •Patients with history of mucositis / osteomathitis Grade II and above based on the definition of the terminology of the incidence of complications
- •Having a condition that affects subcutaneous fentanyl tolerance or absorption of buccal mucosa
- •Pregnancy / Breastfeeding
- •Sleep apnea
- •Active metastasis in the brain by increasing intracranial pressure
- •Chronic lung obstruction
- •Renal or liver dysfunction
- •Brady's remarkable arrhythmias have not been diagnosed with heart disease
- •Any sudden increase in unrelated cancer pain
- •Conscious unwillingness to participate in the study
研究者
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