A Comparative Analysis of Intertransverse Nerve Block and Paravertebral Nerve Block in Endoscopic Hepatectomy
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Pain
- Sponsor
- Jie Chen
- Enrollment
- 80
- Locations
- 1
- Primary Endpoint
- The number of effective compressions of the analgesic pump within 24 hours after surgery
- Status
- Active, not recruiting
- Last Updated
- last year
Overview
Brief Summary
This study aims to compare the analgesic effect of intertransverse nerve block and paravertebral nerve block after endoscopic hepatectomy, evaluate its effectiveness and safety, and provide new ideas and clinical basis for postoperative pain management of liver surgery.
Detailed Description
This study was a prospective, double-blind, randomized controlled trial. Patients who were eligible for laparoscopic partial liver resection in our center were included, with intertransverse nerve block as the experimental group and paravertebral nerve block as the control group. Through the analysis of postoperative pain score 30min to 24h, the number of effective analgesic pump compressions within 24h, the amount of analgesic drugs used, complications and other data, To evaluate the efficacy and safety of intertransverse nerve block in patients undergoing laparoscopic partial liver resection.
Investigators
Jie Chen
临床教授
The Second Affiliated Hospital of Chongqing Medical University
Eligibility Criteria
Inclusion Criteria
- •1.18-80 years old adult, BMI\<27.9kg/m2
- •American Society of Anesthesiologists ASA Grade I-III
- •Patients with laparoscopic partial liver resection such as liver tumors
- •Willing to participate in this study and sign the informed consent form
Exclusion Criteria
- •The patient or family member refuses to sign the informed consent form
- •Blood coagulation dysfunction, local infection
- •Those who have communication, communication disorders or mental abnormalities
- •Patients with severe heart, pulmonary and renal insufficiency or patients with central system diseases
- •For any reason, it cannot be matched with the study or the researcher believes that it is not appropriate to be included in this experiment.
Outcomes
Primary Outcomes
The number of effective compressions of the analgesic pump within 24 hours after surgery
Time Frame: Within 24 hours after the operation