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临床试验/ITMCTR2026001738
ITMCTR2026001738进行中(未招募)Unknown

Study on Formulation and Clinical Verification of Standardized Protocol for Transcutaneous Electrical Acupoint Stimulation in Promoting Postoperative Gastrointestinal Function Recovery After Peritoneal Cancer Surgery

Beijing Shijitan Hospital, Capital Medical University0 个研究点开始时间: 2026年7月31日最近更新:
适应症

试验速览

阶段
Unknown
状态
进行中(未招募)
发起方

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 至 75(—)
性别
All

入选标准

  • (1) Patients with primary peritoneal carcinoma or peritoneal metastasis confirmed by imaging combined with pathological or cytological examination, who are planned to receive CRS+HIPEC;
  • (2) Age ranging from 18 to 75 years old;
  • (3) Body mass index (BMI): 18–31 kg/m²;
  • (4) American Society of Anesthesiologists (ASA) physical status classification Grade I–III;
  • (5) Voluntarily participate after full informed consent and sign the written informed consent form.

排除标准

  • (1) Scarring, skin infection or sensory disturbance on the skin surrounding target acupoints (Zusanli, Shangjuxu, Hegu, Neiguan);
  • (2) Pre-existing peripheral nerve injury or prior spinal surgery history;
  • (3) Implanted electronic devices such as cardiac pacemakers;
  • (4) Preoperative intestinal obstruction or severe gastrointestinal motility disorders;
  • (5) Long-term preoperative use of analgesic medications;
  • (6) Confirmed psychiatric or neurological disorders;
  • (7) Requirement for intraoperative colostomy;
  • (8) Cognitive dysfunction precluding cooperation with treatment and outcome assessments.

研究者

发起方
Beijing Shijitan Hospital, Capital Medical University

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