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临床试验/TCTR20230224001
TCTR20230224001招募中2 期

Comparison between intravenous fluid deficit replacement and non deficit replacement at operating room in gynecological patients undergoing surgery

/A0 个研究点目标入组 230 人开始时间: 2023年2月24日最近更新:
适应症

试验速览

阶段
2 期
状态
招募中
发起方
入组人数
230

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 Years 至 65 Years(—)
性别
Female

入选标准

  • •1. ASA Class1, 2, age 18 to 65 years old A gynecological patient underwent a low midline incision (under the navel) for non-invasive tumor surgery
  • •2. underwent non-urgent surgery (elective surgery)
  • •3. hematocrit more than 30% Hb more than 10 g/d
  • •4. Blood osmolarity 280 + 6 mOsm/L
  • •5. The patient withholds water and food after midnight

排除标准

  • •1. Use for more than 3 hours, except for skin incision.
  • •2. There must be bleeding between the blood volume greater than 20%.
  • •3. If 3rd ventricle loss > 20% of estimated blood loss (EBL)
  • •4. If the anesthesiologist decides that the patient cannot participate in the program Patients will be excluded from the program

研究者

发起方
/A

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