2024-03-01
2025-08-31
2025-12-31
60
NCT06214533
Sixth Affiliated Hospital, Sun Yat-sen University
Sixth Affiliated Hospital, Sun Yat-sen University
INTERVENTIONAL
Celiac plExus Block to Reduce OpioID Consumption Following Hepato-pancreato-biliary Mini-invasive Surgery
The goal of this study is to assess the efficacy of intraoperative celiac plexus block (CPB) to reduce opioid consumption following laparoscopic hepato-pancreato-biliary surgery
A bilateral CPB is convenient and safe to perform under the direct laparoscopic vision of the surgeons during surgery; however, perspective data are warranted. The investigators hypothesize that a bilateral CPB using 0.5% ropivacaine will improve the quality of recovery following a laparoscopic hepato-pancreato-biliary surgery. The primary endpoint is the Postoperative opioid use. Secondary endpoints include acute postoperative pain, opioid consumption, the incidence of postoperative nausea or vomiting (PONV), the 15-item quality of recovery questionnaire (QoR-15), length of post-anesthesia care unit (PACU) stay, length of post-operative hospital stay, and chronic post-surgical pain at 90 d after surgery.
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Registration Dates | Results Reporting Dates | Study Record Updates |
---|---|---|
2023-04-03 | N/A | 2024-01-10 |
2024-01-10 | N/A | 2024-01-19 |
2024-01-19 | N/A | 2024-01 |
This section provides details of the study plan, including how the study is designed and what the study is measuring.
Primary Purpose:
Treatment
Allocation:
Randomized
Interventional Model:
Parallel
Masking:
Quadruple
Arms and Interventions
Participant Group/Arm | Intervention/Treatment |
---|---|
EXPERIMENTAL: Never block Prior to the end of the laparoscopic surgery and any additional procedures, the bilateral celiac plexus block will be performed by the surgeon after identification of the aorta at the superior border of body of pancreas. A 22-gauge spinal needle will be i | DRUG: Ropivacaine 0.5%
|
PLACEBO_COMPARATOR: Placebo block Patients in the control arm will undergo the celiac plexus block procedure as well. The block will contain 20 ml of 0.9% normal saline + 1:400000 adrenaline. Intervention: Drug: 20 mL of 0.9% normal saline | DRUG: Normal Saline
|
Primary Outcome Measures | Measure Description | Time Frame |
---|---|---|
Postoperative opioid use | The primary outcome will be morphine equivalent during the first postoperative 24 h | Up to 24 h after surgery |
Secondary Outcome Measures | Measure Description | Time Frame |
---|---|---|
Postoperative opioid use | Patients will be recorded for up to 72 h postoperative opioid consumption. | Up to 72 h after surgery |
Numeric rating scale (NRS) for pain | Patients will be asked to complete a daily diary up to 72 h that records numeric pain rating scale | Up to 72 h after surgery |
Postoperative vomiting | Incidence of postoeprative vomiting will be recorded for up to 72 h | Up to 72 h after surgery |
Quality of recovery using the 15-item quality of recovery questionnaire (QoR-15) | Patients will be asked to complete a 15-item quality of recovery questionnaire up to 72 h after surgery | Up to 72 h after surgery |
Post-anesthesia care unit (PACU) time | Length of PACU stay | Through study completion, an average of 1 year |
Post-operative hospital time | Length of hospital stay | Through study completion, an average of 1 year |
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact Name: Hu Phone Number: +8613500000368 Email: 1372351078@qq.com |
Study Contact Backup Name: Guo Phone Number: +8613660859897 Email: Jingguo17@163.com |
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person’s general health condition or prior treatments.
Ages Eligible for Study:
ALL
Sexes Eligible for Study:
18 Years
Accepts Healthy Volunteers:
This is where you will find people and organizations involved with this study.
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General Publications
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