Perioperative analgesia and postoperative rehabilitation
Conditions
Interventions
Cheek Acupuncture Combined with Ropivacaine Incision Infiltration Group:After general anesthesia intubation, cheek acupuncture will be performed, and ropivacaine incision infiltration will be carried
Ropivacaine Incision Infiltration Group:No acupuncture treatment will be given. Ropivacaine incision infiltration will be performed before incision suturing.
Paravertebral Block Group:Paravertebral nerve block will be performed after general anesthesia and intubation.
Sponsors
155 Nanjing North Street, Heping District, Shenyang City, Liaoning Province, China
Eligibility
Sex/Gender
All
Age
18 Years to 70 Years
Inclusion criteria
Inclusion criteria: (1) Patients scheduled for thoracoscopic surgery under general anesthesia; (2) Age ranging from 18 to 70 years at the time of enrollment; (3) American Society of Anaesthesiologists (ASA) physical status class I to III; (4) 18kg/m ^ 2 = body mass index (BMI) = 24kg/m ^ 2; (5) Surgical time less than 5 hours; (6) Unilateral surgery; (7) Thoroughly understand the experiment and voluntarily sign the informed consent form.
Exclusion criteria
Exclusion criteria: (1) Patients who refuse to participate in the study; (2) Patients with abnormal coagulation function; (3) Patients with infected or ruptured skin at the acupuncture points; (4) Patients with a history of chronic pain (lasting for more than 3 months) or continuous use of analgesics within 2 weeks before surgery; (5) Patients with drug abuse or alcohol dependence; (6) Patients with a history of severe liver, kidney or heart abnormalities within the past six months; (7) Patients with severe visual or auditory deficiencies; (8) Patients with consciousness disorders or mental or neurological diseases and unable to cooperate; (9) Patients who have undergone thoracotomy in the past; (10) Patients with lung diseases such as pulmonary infections and asthma. (11) Patients who convert to thoracotomy or be transferred to the intensive care unit after surgery;
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Total opioid consumption within the first 24 postoperative hours; | — |
Secondary
| Measure | Time frame |
|---|---|
| Time to first rescue opioid administration;Number of rescue opioid administrations within 24 hours;Pain at rest (numerical rating scale);Movement-evoked pain (numerical rating scale);Pain Score at 3 Months Postoperatively;Ramsay Sedation Scale;Opioid-related adverse events;Procedure-related complications;Awakening due to pain (Yes/No);Ambulate independently (Yes/No);Passing flatus (Yes/No);Length of stay; | — |
Countries
China
Contacts
Public ContactBao Naren
First Affiliated Hospital of China Medical University
Outcome results
None listed