thoracic surgery
Conditions
Interventions
control group:NONE
Sponsors
Shanghai Chest Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 75 Years
Inclusion criteria
Inclusion criteria: (1) Both male and female, aged 18-75 years old, volunteered to sign the informed consent for the study; (2) patients undergoing thoracoscopic pneumonectomy under general anesthesia; (3) ASA I-II;
Exclusion criteria
Exclusion criteria: (1) patients who have undergone surgery along the meridian line; (2) patients with local skin infection of acupoints; (3) patients with upper or lower limb nerve injury; (4) patients with a history of long-term use of sedative, analgesic or antidepressant drugs; (5) patients unable to finish the study, including language difficulties, infectious diseases, and other medical history.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| mean pain intensity over the first 24 hours after the operation, as measured by VAS score; | — |
Secondary
| Measure | Time frame |
|---|---|
| Incidence of nausea and vomiting;QoR-15 score at 24 h after surgery;type and dosage of analgesics needed;VAS score at each time point (1 hours,12 hours, and 24 hours) after the operation;the incidence of postoperative chest related complications;incidence of non-discharge within 24 hours after the operation;total length of hospital stay; | — |
Countries
China
Contacts
Public Contactwujingxiang
Shanghai Chest Hospital
Outcome results
None listed