The effect of transcutaneous electrical acupoint stimulation on catheter- related bladder discomfort in resuscitation patients undergoing thoracic surgery

Phase 1

• Conditions: catheter- related bladder discomfort

• Registration Number: ITMCTR2200006132
• Lead Sponsor: Affiliated Tumor Hospital of Guangzhou Medical University

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 elective pulmonary surgery or mediastinal esophageal surgery under general anesthesia.Surgical types include:wedge resection of lung,pneumonectomy,mediastinal tumor resection and diagnostic pleura resection,radical resection of esophageal cancer,with no surgical methods(thoracotomy or VATS);
(2)18-60 years old;
(3)BMI:18-25;
(4)American Society of Anesthesiologists(ASA) Rating:?-?;
(5)fully understand the test plan and purpose and sign the informed consent.

Exclusion Criteria

(1)Mental system diseases(such as schizophrenia,depression,etc.)and cognitive dysfunction.
(2)Patients with serious cardiovascular and cerebrovascular diseases(such as myocardial infarction,unstable angina pectoris,stroke with sequelae,etc.);
(3)Patients with urethral malformation,annulus urethra,prostatic hyperplasia or prostate diseases;
(4)Infection at the needle site or previous operation marks;
(5)Postoperative unplanned admission to ICU or secondary endotracheal intubation or surgery;
(6)The subject and his/her family decide to withdraw the informed consent for any reason;
(7)Occurrence of serious clinical adverse events,abnormal laboratory tests,or concomitant diseases that make the subject unsuitable for further study;
(8)Patients who need to change the way of surgery or anesthesia due to various reasons during the operation;
(9)Sterward score=4 points during 10 minutes after the end of electrical stimulation.

Study & Design

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

Primary Outcome Measures

Name	Time	Method
Severity of catheter- related bladder discomfort;