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临床试验/NCT04732234
NCT04732234Unknown不适用

Pre-emptive Ultrasound Guided Superior Hypogastric Plexus Block in Pelvic Cancer Surgeries : a Randomized Double-Blinded Study

National Cancer Institute, Egypt1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2020年12月1日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
40
试验地点
1
主要终点
morphine consumption

研究概览

简要总结

The superior hypogastric plexus (SHP) is a retroperitoneal structure with a predominance of afferent sympathetic nerve fibers. The perception of central pelvic pain is thought mainly to involve transmission through this plexus. Therefore, blocking or of SHP has been used to treat pelvic pain.

详细描述

Ultrasound guided superior hypogastric plexus block there is 2 equal groups:

Group S (SHPB group 18 patients) ultrasound guided SHPB is done after induction of balanced general anesthesia (fentanyl, propofol and rocuronium) using 20 ml Bupivacaine 0.5% before skin incision, Group C (Control group 18 patients) in which same technique will be done but using normal saline 0.9% instead of bupivacaine. Patients of both groups will receive patient controlled analgesia using morphine with continous background infusion of morphine 1.5 mg/h with adding granisterone 2mg/60 ml and ability to give bolus of 0.5 mg morphine on demand.

• Dosing and administration; Group S (SHPB group 18 ultrasound guided SHPB ) using 20 ml Bupivacaine 0.5% before skin incision.

Group C (Control group 18 patients) in which same technique will be done but using normal saline 0.9%

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 (Participant, Investigator)

盲法说明

Randomization is done using computer generated sequence. Concealment will be achieved by opaque envelope.

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • ASA II,III.
  • Patients undergoing pelvic surgeries.

排除标准

  • Patients refusal,
  • Coagulopathy,
  • Infection.

结局指标

主要结局

morphine consumption

时间窗: baseline till 24 hours postoperative

Total 24 hours morphine consumption in milligrams

次要结局

  • Visual analogue scale (VAS)(Visual analogue scale (VAS) at baseline till 24 hours postoperative)

研究者

发起方
National Cancer Institute, Egypt
申办方类型
Other
责任方
Principal Investigator
主要研究者

Mohammed Abdelfattah Abdelwadod

Mohammed Abdelfattah Abdelwadod

National Cancer Institute, Egypt

研究点 (1)

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