Effects of Transcutaneous Electrical Acupoint Stimulation on emergence agitation and inflammatory cytokines in patients undergoing thoracoscopic surgery
- Conditions
- lung disease
- Registration Number
- ITMCTR2100004892
- Lead Sponsor
- Hebei General Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- Not specified
1. Patients who intend to undergo thoracoscopic surgery under general anesthesia;
2. Aged 25-70 years, gender and weight are not limited;
3. American Society of Anesthesiologists ASA classification I-III, no history of serious systemic diseases;
4. The operation time is estimated to be about 2 hours;
5. Those who agree to accept this trial and sign an informed consent form.
1. Those who have local infection or chronic inflammation on the surface of the acupoint stimulation site, or who cannot stick electrode pads;
2. The adjacent nerves of acupoints such as median, ulnar and radial nerves are confirmed to have functional impairment and hypoesthesia due to cervical spondylosis or trauma;
3. It is expected that there is a difficult airway (such as abnormal airway grading, menthol spacing, mouth opening, etc.) or difficult extubation or short-term failure to extubate the tube due to the patient's own factors;
4. Those who have recently received acupoint stimulation or treatment or have been significantly insensitive to acupoint stimulation treatment in the past;
5. Severe lung infection, bronchial inflammation, high airway response, and large amount of sputum are expected to have a greater impact on postoperative extubation.
Study & Design
- Study Type
- Interventional study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Interleukin 6;Interleukin 10;
- Secondary Outcome Measures
Name Time Method