Postoperation pain
Conditions
Interventions
Experimental group:continous intercoastal nerve block
control group :Continuous patient controlled intravenous analgesia
Sponsors
The Affiliated Hosptia of Qingdao University
Eligibility
Sex/Gender
All
Age
18 Years to 75 Years
Inclusion criteria
Inclusion criteria: 1. The patients who voluntarily participate in the study shall sign the informed consent form by themselves or their legal representatives (when necessary); 2. Patients with Asai ~ II grade; 3. Patients aged 18-75 years, regardless of gender; 4. Patients who underwent lobectomy (single or double lobed) and systematic lymph node dissection; 5. Be able to understand vas and PCIA usage; 6. All of the above are included, and those who are not are excluded.
Exclusion criteria
Exclusion criteria: 1. The patients who received chemotherapy and radiotherapy before operation; 2. Patients with severe cardiovascular and cerebrovascular disease or neuromuscular disease history; 3. Patients with long-term use of narcotic analgesics, sedatives or NSAIDs; 4. Patients who cannot cooperate with the study for any reason, such as language understanding, mental illness; 5. The researchers think that other reasons are not suitable for the subjects of clinical trials.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The quality of life;VAS; | — |
Secondary
| Measure | Time frame |
|---|---|
| The quality of sleep;DAAS-21; | — |
Countries
China
Contacts
Public ContactJianfang Song
The Affiliated Hosptia of Qingdao University
Outcome results
None listed