postoperative pain
Conditions
Interventions
The observation group:Conventional analgesic treatment (nonsteroidal anti-inflammatory drugs)+borneol-alcohol solution wet compress for postoperative pain
The control group:Conventional analgesic treatment (nonsteroidal anti-inflammatory drugs)
Sponsors
Yantaishan Hospital,Yantai
Eligibility
Sex/Gender
All
Age
18 Years to 70 Years
Inclusion criteria
Inclusion criteria: (1) Age between 18 and 70 years; (2) Undergoing thoracoscopic lobectomy for the first time; (3) Pathological type is non-small cell lung cancer; (4) No long-term use of psychiatric or analgesic medications.
Exclusion criteria
Exclusion criteria: (1) Impaired consciousness or uncooperative behavior; (2) Pre-existing pain before surgery; (3) Concurrent other malignant tumors or life-threatening diseases; (4) Alcohol allergy; (5) Movement disorders of the limbs or severe osteoarthritis and other contraindications for movement.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| the Numerical Rating Scale (NRS) scores at rest and during movement; | — |
Secondary
| Measure | Time frame |
|---|---|
| the symptom cluster burden scores using the validated Chinese version of M.D. Anderson Symptom Inventory-Lung cancer (MDASI-L) and the 6-minute walking distance (6MWD) at 24-hour postoperative.;the frequency of supplemental NSAID administrations and rescue dezocine interventions during the initial 48-hour postoperative period; | — |
Countries
China
Contacts
Public ContactMeiyun Lou
Yantaishan Hospital,Yantai
Outcome results
None listed