Combined General and Spinal Anesthesia vs. General Anesthesia for Pain Relief During Laparoscopy Gynecological Surgery
试验速览
- 阶段
- 不适用
- 入组人数
- 40
- 试验地点
- 3
- 主要终点
- Pain level
研究概览
简要总结
The purpose of this study is to determine whether combined anesthesia will provide better pain control for the postoperative period following gynecological laparoscopy surgery.
详细描述
Following signing an informed consent patients who are scheduled for gynecological laparoscopy surgery for benign disease will randomized to general vs. combined general and spinal anesthesia.
During the postoperative period data regarding pain level as evaluated by visual analogue scale (VAS), number of doses of pain relief drugs, satisfaction and number of day in hospitalization will be collected from patient charts.
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
- Single (Investigator)
入排标准
- 年龄范围
- 18 Years 至 70 Years（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •American Society of Anesthesiology (ASA) physical status classification system:ASA I-III.
- •Benign Gynecological Laparoscopy surgery
排除标准
- •Patients who are not capable to sign the consent form.
- •Women with known allergy to the medication used in spinal analgesia.
- •Patients who are pregnant or lactating.
- •Patients with contraindication to spinal analgesia.
- •Patients who use opioid on a regular base.
结局指标
主要结局
Pain level
时间窗: For the first 72 hours following surgery
Pain level will be evaluated every 4 hours from the time of surgery to discharge
Number of doses of analgesic drugs
时间窗: For the first 72 hours following surgery
Number of doses of analgesic medications will be collected from patients charts.
次要结局
未报告次要终点