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

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

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2200006132
Enrollment
Unknown
Registered
2022-06-15
Start date
2022-06-01
Completion date
Unknown
Last updated
2023-02-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

catheter- related bladder discomfort

Interventions

2:transcutaneous electrical acupoint stimulation

Sponsors

Affiliated Tumor Hospital of Guangzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion 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

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.

Design outcomes

Primary

MeasureTime frame
Severity of catheter- related bladder discomfort;

Countries

CHINA

Contacts

Public ContactShuixian Ye

Affiliated Tumor Hospital of Guangzhou Medical University

847548748@qq.com18122154377

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 4, 2026