Effect of transcutaneous acupoint electrical stimulation on hemodynamics and prognosis of patients undergoing lung cancer surgery

Phase 1

• Conditions: Hemodynamics and prognosis of patients undergoing lung cancer surgery

• Registration Number: ITMCTR2100005215
• Lead Sponsor: The Second Affiliated Hospital of Air Force Medical University (Tangdu Hospital)

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 20 February 2023

Recruitment & Eligibility

• Status: Pending
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

1)Patients undergoing lung cancer surgery
2)Age 18-64 years old
3)BMI index 18-30kg/?;
4)American Society of Anesthesiology (ASA) score I-II;
5)No radiotherapy or chemotherapy before surgery;
6)Patients who volunteered for the study;

Exclusion Criteria

1)Communication barriers and unable to cooperate
2)People with a history of depression, anxiety, mental disorders and other psychological and psychiatric diseases
3)A history of chest surgery or a history of chronic pain;
4)Those who are confirmed/suspected to have a history of alcohol, analgesic or other drug abuse and addiction;
5)Those who are contraindicated for transcutaneous electrical stimulation, including those with local skin damage, infection, or implantation of electrophysiological devices in the body;
6)Patients with unstable angina, myocardial infarction and past arrhythmia within 3 months;
7)Preoperative visit blood pressure =180/110 mmHg (WHO-ISH Hypertension Guideline 3 hypertension);
8)Diabetic patients with diabetic complications and poor blood sugar control;
9)COPD GOLD grade III and IV, pulmonary fibrosis, uncontrolled asthma;
10)Use lung isolation methods other than DLT (such as difficult airway, tracheotomy, occluder, artificial pneumothorax);
11)Participated in other clinical trials within 3 months before being selected for the study;
12)The doctor in charge or the investigator believes that there are other situations that are not suitable for participating in this study (the reason needs to be recorded).

Study & Design

• Study Type: Interventional study
• Study Design: Not specified