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临床试验/TCTR20221123003
TCTR20221123003已完成4 期

Incident of Hypotension after Performing Spinal Anesthesia during Preloading of Fluid Gelatin and Phenylephrine during spinal anesthesia Compared with those with Only Fluid Gelatin in Patients undergoing Cesarean Section

Chaiyaphum hospital0 个研究点目标入组 84 人开始时间: 2022年11月23日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
84

研究概览

简要总结

The GP group had less hypotension at intraoperative period than the G group, but this was not statistically significant (40.5 percent and 57.1 percent, p 0.190). When different factors (blood loss, high anesthetic level) were adjusted difference, the GP group had hypotension less than the G group 21.06 percent with statistical significance.

研究设计

研究类型
Interventional

入排标准

年龄范围
18 Years 至 44 Years(—)
性别
Female

入选标准

  • 1. Pregnancy undergoing to ceasarean section and GA 37-40 wk
  • 2. Spinal anesthesia

排除标准

  • 1. complication of obstetric condition, risk bleed over 1000 mL
  • 2. PIH, HT, renal failure, CHF, heart disease, arrhythmia, DM, coagulopathy or thrombocytopenia, asthma, OSA, thyroid disease, liver disease, use MAOI, other drugs that prolonged heart conduction
  • 3. Abnormal of fetus
  • 3. Postural hypotension un-correct
  • 4. Body weight less than 50 kg or more than 80 kg, BMI over 35 kg/m2
  • 5. BP over 140/90 mmHg, SBP less than 90 mmHg, HR less than 60 /min
  • 6. Sensitivity to phenylephrine or fluid gelatin
  • 7. Deny to study

研究者

发起方
Chaiyaphum hospital

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