NCT00233857已完成2 期
Auricular Acupuncture Versus Placebo (Sham Acupuncture) for Postoperative Pain Relief After Ambulatory Knee Arthroscopy - a Randomized Controlled Trial
University Medicine Greifswald2 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2003年8月1日最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 120
- 试验地点
- 2
- 主要终点
- Postoperative ibuprofen requirement after the surgery
研究概览
简要总结
The aim was to investigate whether auricular acupuncture is superior to sham acupuncture in relief of acute postoperative pain and in reduction of analgesics consumption on demand and their side effects in patients after ambulatory knee arthroscopy
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Double
入排标准
- 年龄范围
- 16 Years 至 65 Years（Child, Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients with an American Society of Anesthesiologists physical status of I to II scheduled for ambulatory knee arthroscopy under general anesthesia.
- •Surgery time does not exceed 60 minutes.
- •Patients without previous opioid and/or psychiatric medication.
- •Patients ranged 16-65 years old.
- •Patients able to use Visual Analogue Scale-100 for pain intensity measurement.
- •Patients who have given informed consent.
排除标准
- •Pregnant or nursing females.
- •Recidivist alcoholics and/or patients with history of psychiatric disease.
- •Local or systemic infection.
- •Age < 16 and > 65 years.
- •Surgery time more than 60 minutes.
- •Inability to use Visual Analogue Scale-
- •Patients consumed opioid medication before surgery.
- •Patients with prosthetic or damaged cardiac valves (s. Potential risks)
- •Patients who are unable to understand the consent form.
结局指标
主要结局
Postoperative ibuprofen requirement after the surgery
次要结局
- Pain intensity assessed by patients on VAS-100 ; total piritramide requirement in anesthesia recovery room; incidence of analgesia-related side effects
研究者
研究点 (2)
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