postoperative pulmonary complications
Conditions
Interventions
Control Group:placebo transcutaneous electrical acupoint stimulation
Sponsors
The First Affiliated Hospital of Wenzhou Medical University
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: Selection criteria: (1) ASAI-III (2) Age 18-60 (3) Weight 40-70 kilograms, (4) Patients undergoing video assisted lung lobectomy
Exclusion criteria
Exclusion criteria: Exclusion criteria: (1) There are surgical incisions or scars on the local and local meridians of the acupoints (2) Patients with local skin infections at acupoints (3) Patients with upper or lower limb nerve damage (4) Have a history of spinal surgery (5) Patients who have participated in other clinical trials within the past four weeks (6) Unable to understand VAS score and NRS score (7) Pacemaker patients (8) Opioid drug addiction and dependence (9) Preoperative complications of severe central nervous system disease and severe mental illness (10) Patients with a history of alcoholism (11) Long term use of hormone drugs (12) The researchers believe that it is not suitable for participants in this experiment.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| postoperative pulmonary complications; | — |
Secondary
| Measure | Time frame |
|---|---|
| NLR;PLR; | — |
Countries
China
Contacts
Public ContactJunlu Wang
The First Affiliated Hospital of Wenzhou Medical University
Outcome results
None listed