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
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