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临床试验/ITMCTR1900002637
ITMCTR1900002637已完成2 期

Clinical study for Xiangbin prescription for promoting recovery of gastrointestinal function after gynecological surgery

The Second Clinical Medical College of Guangzhou University of Traditional Chinese Medicine0 个研究点开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
已完成
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional study

入排标准

年龄范围
18 至 65(—)
性别
Female

入选标准

  • 1. Undergone gynecological laparoscopic surgery;
  • 2. Aged between 18 and 65 years old;
  • 3. Operation duration 0.5–4.5 h;
  • 4. Anesthesia duration 1.0–5.0 h;
  • 5. TCM syndrome Qi deficiency, Qi stagnation, blood stasis and bowel-qi?obstruction;
  • 6. Provided informed consent.

排除标准

  • 1. Advanced malignant tumor cachexia or extreme weakness;
  • 2. Malignant tumors requiring extended radical surgery;
  • 3. Serious cardiovascular, liver, kidney, brain, lung co-morbidity and other combined diseases;
  • 4. Mental illness;
  • 5. Hypertension or diabetes poorly controlled by drugs;
  • 6. Allergic to the intervention;
  • 7. Pregnant or breast-feeding women;
  • 8. Severe malnutrition defined as serum albumin < 21g/L; pre-albumin < 0.10g/L;
  • 9. Hypertension or diabetes poorly controlled by drugs;
  • 10. Need for second abdominal surgery with severe intestinal adhesion;
  • 11. Serious complications occurring within 6 hours after surgery(e.g., multiple organ dysfunction);
  • 12. Postoperative intraperitoneal hyperthermic perfusion;
  • 13. Have undergone emergency surgery;
  • 14. Need for other gastroprokinetic drugs after surgery;
  • 15. Current participation in or past participation in other clinical trials within one month prior to this study;
  • 16. Considered inappropriate to participate in this study by the clinical investigators;
  • 17. Need for blood transfusion; blood loss during surgery > 400 mL.

研究者

发起方
The Second Clinical Medical College of Guangzhou University of Traditional Chinese Medicine

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