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Clinical Trials/ITMCTR2100005469
ITMCTR2100005469Recruiting未知

Transcutaneous acupoint electrical stimulation improves postoperative sleep of patients with gastrointestinal tumors by regulating the Nrf2/ARE signal pathway

Xuzhou Traditional Chinese Medicine Hospital Affiliated to Nanjing University of Chinese Medicine0 sitesStarted: TBDLast updated:
Conditions

Trial Snapshot

Phase
未知
Status
Recruiting
Sponsor

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional study

Eligibility Criteria

Ages
18 to 75 (—)
Sex
All

Inclusion Criteria

  • 1.Patients undergoing elective laparoscopic gastrointestinal tumor surgery
  • 2.Age: 18 to 75 years old
  • 3.American Association of Anesthesiologists (ASA) grade I to III
  • 4.BMI 18.5kg/m2 - 28kg/m2
  • 5.Preoperative clinical tumor TNM staging: cTis-3N0-1M0 (refer to AJCC/UICC 8th edition TNM staging)

Exclusion Criteria

  • 1. PSQI>7 points. 2.Sleep apnea, or moderate or more snoring. 3. Preoperative sinus bradycardia (heart rate less than 50 beats/min) or sinus node disease, second-degree or third-degree atrioventricular block, and pacemaker. 4.Long-term use of anticonvulsants, antidepressants or other psychotropic drugs. 5. Those who are highly sensitive or allergic to the drugs or equipment in this study. 6.Severe heart, liver or kidney disease. 7. Participated in other clinical trials in the past 3 months. 8.Hearing and language communication barriers, unable to communicate effectively with doctors. 9. Patients who are pregnant or breastfeeding. 10.Patients with fever or infection before surgery.11.Patients who live with critically ill patients or live in a ward with> 3 persons.

Investigators

Sponsor
Xuzhou Traditional Chinese Medicine Hospital Affiliated to Nanjing University of Chinese Medicine

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