EUCTR2013-004219-36-AT进行中（未招募）不适用
Magnetic Resonance Imaging of Local Anesthetic Distribution: A Comparison of 5 and 15 milliliters of ropivacaine 0.75% for ultrasound guided interscalene plexus blockade - MR-ISB
Paracelsus Mediznische Privatuniversität, Universitätsklinik für Anästhesiologie, perioperative Medizin und Intensiv0 个研究点开始时间: 2013年10月22日最近更新:
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
- All
入选标准
- •- Age between 18 and 75 years
- •- Surgery of the shoulder (shoulder arthroscopy, open shoulder joint surgery, rotator cuff surgery, tendon transfer, shoulder arthroplasty, humerus fracture surgery)
- •- Informed consent to participate in the study
- •- American Society of Anesthesiologists physical score I, II or III
- •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 20
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 10
排除标准
- •- Refusal to participate in the study
- •- Inability to understand the study protocol due to language barrier
- •- Serious cardiac or pulmonary disease such as decompensated heart failure, recent myocardial infarction (less than one month in the past), heart block greater than 2nd degree, obstructive sleep apnea and chronic obstructive lung disease greater than 2nd degree
- •- renal impairment with an aGFR < 60ml/min
- •- Hypersensitivity to ropivacaine or gadolinium or other contraindications against peripheral nerve blocks
- •- Chronic opioid usage greater than 15 mg oral morphine equivalents daily, the daily use of adjunctive pain medications (gabapentinoids, tricyclic antidepressants, serotonin-norepinephrine reuptake inhibitors)
- •- Schizophrenia or bipolar disorders, uncontrolled anxiety, claustrophobia
- •- Peripheral neuropathy
- •- Hepatic or renal impairment
- •- Ongoing illicit drug or alcohol abuse
- •- Metal implants or other contraindications for magnetic resonance imaging
- •- Coagulopathy
- •- Participation in additional clinical trials within 4 weeks before screening
- •- Hearing impairment
- •- Pregnancy
研究者
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