EUCTR2006-003737-33-SE进行中（未招募）不适用
Continuous Intraperitoneal Infusion of Local Anesthetics vs. Patient Controlled Intraperitoneal injection for Postoperative Pain relief following Abdominal Hysterectomy. A randomized, double-blind study
Örebro University Hospital0 个研究点开始时间: 2006年9月7日最近更新:
适应症
相关药物
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
- Female
入选标准
- •18 –65 year old patients undergoing open abdominal hysterectomy.
- •Have signed and dated Informed Consent.
- •Willing and able to comply with the protocol for the duration 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
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Patients undergoing open abdominal hysterectomy due to suspected cancer.
- •Patients with chronic pain who are taking analgesics regularly.
- •Allergy to components in levobupivacaine (Chirocaine)/Saline (Sodium Chloride).
- •Participation in other clinical trials.
研究者
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