The patient experienced acute pain after the operation
Conditions
Interventions
Control group (Group P):Ultrasound-guided paravertebral block
Experimental group (Group R):Ultrasound-Guided Rhomboid Intercostal and Sub-Serratus Plane Block
Experimental group (Group I):Ultrasound- Guided Intertransverse Process Block
Sponsors
chongqing university cancer hospital
Eligibility
Sex/Gender
All
Age
18 Years to 75 Years
Inclusion criteria
Inclusion criteria: 1. Aged 18 to 75 years, with ASA classification of I to III; 2. Plan to undergo elective unilateral thoracoscopic surgery (such as lobectomy, segmentectomy, or wedge resection of the lung); 3. Voluntarily participate in this trial and sign the informed consent form.
Exclusion criteria
Exclusion criteria: 1. Coagulation dysfunction; 2. Infection at the puncture site; 3. History of allergy to local anesthetics; 4. Patients with a BMI of 32 or above; 5. Patients who have been using opioid drugs for a long time or who have chronic pain before the surgery; 6. Severe cardiac or pulmonary dysfunction or abnormal liver and kidney functions; 7. Patients with cognitive dysfunction or those unable to understand NRS scores; 8. Patients with spinal injuries.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postoperative NRS pain score; | — |
Secondary
| Measure | Time frame |
|---|---|
| Record oCharacteristics of Nerve Block Performance;QoR-15 score;The dosage of opioid drugs within 24 hours after the operation.;The dosage of opioid drugs used during the operation.; | — |
Countries
China
Contacts
Public ContactXiao-Long Liang
chongqing university cancer hospital
Outcome results
None listed