ACTRN12612000981820尚未招募未知
A double blinded randomised controlled trial assessing and comparing the total average 24 to 48 hour post surgical morphine usage and analgesic quality of 3 types of abdominal wall block catheters (transversus abdominis plane versus rectus sheath plane versus subcutaneous plane) in participants receiving midline laparotomy for gynaecological oncology surgery.
Mater Health Services0 个研究点目标入组 90 人开始时间: 2012年9月12日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 发起方
- 入组人数
- 90
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- Female
入选标准
- •Women who are undergoing a laparotomy for gynaecological oncology procedures with an expected midline incision.
排除标准
- •Conditions associated with opioid tolerance: regular opioid analgesia use in the last three months, previous IVDU
- •Abdominal wall block technically difficult to perform: eg obesity (BMI > 35)
- •Contraindication to abdominal wall block: local sepsis, local anaesthetic allergy, abnormal anatomy (for example nephrectomy scars)
- •Preference for other technique for postoperative analgesia, such as epidural infusion.
- •Presence of stoma
- •Age less than 18.
- •Inadequate capacity to consent
研究者
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