ITMCTR2200006132
Not yet recruiting
Phase 1
The effect of transcutaneous electrical acupoint stimulation on catheter- related bladder discomfort in resuscitation patients undergoing thoracic surgery
Affiliated Tumor Hospital of Guangzhou Medical University0 sitesTBD
Conditionscatheter- related bladder discomfort
Overview
- Phase
- Phase 1
- Intervention
- Not specified
- Conditions
- catheter- related bladder discomfort
- Sponsor
- Affiliated Tumor Hospital of Guangzhou Medical University
- Status
- Not yet recruiting
- Last Updated
- 3 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
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.
Outcomes
Primary Outcomes
Not specified
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