EUCTR2014-004725-40-ES进行中(未招募)不适用
Interfascial effectiveness of ultrasound-guided blocking in transurethral resection of bladder tumor
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中(未招募)
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
- •1. Adult patients of both genre aged between 18 and 85 years, BMI less than 40.
- •2. Bladder tumor diagnosed by ultrasound and / or flexible cystoscopy candidate for surgery transurethral resection of bladder tumor side face within three months of diagnosis.
- •3. Single or multi-level lesion located anterior quadrant of the side faces bladder.
- •4. Clinical indication for transurethral resection (TUR) of bladder tumor.
- •5. Patients who signed informed consent indicating that they have been informed of all pertinent aspects of the trial.
- •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 30
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 52
排除标准
- •1. Physical State assessed by ASA> 4 and / or ECOG> 4
- •2. Allergy or hypersensitivity to lidocaine or any of the excipients of the study drug.
- •3. Pregnant or breast-feeding.
- •4. Participation in a clinical drug research before 3 months in pre-drug administration.
- •5. Concomitant use of the following drugs: amiodarone, disopyramide, phenobarbital, phenytoin, monoaminooxidas inhibitors.
- •6. Subjects with contraindications for regional anesthesia: patient refusal, skin infection, severe neurology pathology, severe thrombocytopenia (platelet count <100,000) receiving both treatment groups.
研究者
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