ISRCTN84820314未知未知
Effectiveness of an audio-visual device for anxiety and pain reduction during a nerve block procedure – a randomized controlled trial
适应症
试验速览
- 阶段
- 未知
- 入组人数
- 99
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
- 性别
- All
入选标准
- •1. Adults 18 years and older
- •2. Conditions that require nerve block intervention
- •3. Written informed consent
- •4. We allow re-enrolment in the randomisation procedure, as some patients will return for repeated treatment during the randomisation period. A new written informed consent is needed
排除标准
- •1. Patients with difficulties in speaking and reading Dutch
- •2. Patients physically or mentally not able to consent
- •3. Patients with severe hearing loss or refraction errors making it impossible to wear the audiovisual device
- •4. Anxiety disorders, such as panic disorder, obsessive-compulsive disorder, posttraumatic stress disorder and others
- •5. ASA 4 - 5
研究者
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