Postoperative pain
Conditions
Interventions
Group R:15 mL 0.375% ropivacaine with 0.1 mg/kg dexamethasone
Group RD1:15 mL 0.375% ropivacaine plus 0.5 µg/kg DEX with 0.1 mg/kg dexamethasone
Sponsors
Liaocheng People's Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Patients aged 45-65 years; 2. Selective surgery patients of undergoing thoracoscopic lobectomy; 3. ASA 1 to 2.
Exclusion criteria
Exclusion criteria: 1. Patients with clinically serious cardiovascular or peptic ulcer diseases; 2. Patients with allergic history to LA, DEX or NSAIDs; 3. Patients with body mass index (BMI) > 30 kg / m2; 4. Patients with infection of puncture site; 5. Patients with chronic pain or analgesic use history in the past 6 months; 6. Patients who cannot use vas or PCIA system.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| the pain both at rest and upon coughing during 72 h after surgery; | — |
Secondary
| Measure | Time frame |
|---|---|
| Prince Henry Hospital Pain Score; hemodynamics; consumption of sufentanil;anesthetized dermatomal distribution; recovery time;total number of presses of the patient controlled intravenous analgesia (PCIA) pump; number of patients needing rescue analgesia; time to first rescue analgesic; total dose of rescue analgesic;;satisfaction scores of patients and surgeon; time of feeding, ambulation, anal exhaust, removal of chest tubes; | — |
Countries
China
Contacts
Public ContactXiujuan Gao
Liaocheng People's Hospital
Outcome results
None listed