跳至主要内容
临床试验/NCT05301127
NCT05301127已完成不适用

Combination of Spinal-Epidural With General Anesthesia in Patients Undergoing Mega-Liposuction Surgery

Cairo University1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2022年1月11日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
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 combination of general anesthesia to spinal and epidural techniques (CSEGA) proved to have a synergistic effect, thus, the use of sub-anesthetic doses can provide satisfactory anesthetic and analgesic results. CSEGA has several known advantages including appropriate postoperative analgesia, shows some benefit in the intraoperative blood loss control causing a decreased need for blood transfusion, rapid regain of the gastrointestinal actions and decreases the incidence of postoperative respiratory complications. Unfortunately, the drawbacks of using neuro-axial anesthesia in combination to general anesthesia will be not thoroughly introduced in many researches, thus, remain unclear.

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, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Inclusion criteria:
  • •Patients aged from 18 to50 years.
  • •ASA I-II.
  • •undergoing elective liposuction surgery
  • •BMI from 25 to 40 kg/m2

排除标准

  • •Patient refusal
  • •ASA III-IV.
  • •Patients aged less than 18 or more than
  • •Body mass index >
  • •Any contraindications to neuro-axial block such as coagulopathy or spine deformity
  • •Chronic opioid consumption,
  • •History of parenteral or oral analgesic intake within the last 48hours.

研究组 & 干预措施

CSEGA group

Active Comparator

Will be received combined spinal-epidural-general anesthesia.

干预措施: spinal-epidural device (Device)

GA group

No Intervention

will be received general anesthesia only.

结局指标

主要结局

morphine consumption

时间窗: 24 hours

postoperative morphine consumption

次要结局

  • Intraoperative surgeon satisfaction.(6 hours)
  • Incidence of complications(24 hours)
  • Blood loss(6 hours)
  • Postoperative patient satisfaction(24 hours)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Amr Samir Wahdan

Lecturer of Anesthesia, Pain management and Surgical ICU

Cairo University

研究点 (1)

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