Opioid consumption at 24 hr post-operation using Morphine Milligram equivalents(MME)
Intraoperative Lidocaine and Combined With Ketamine on Opioid After Bariatric Surgery
Brief Summary
Intervention / Treatment
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Lidocaine Hydrochloride (DRUG)lidocaine will be given 1.5 mg/kg bolus at induction then 2mg/kg/hr until the end of surgery.
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Ketamine (DRUG)Ketamine will be given 0.35 mg/kg bolus at induction then 0.2 mg/kg/hr until the end of surgery.
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Placebo (DRUG)Normal saline will be given with the same rate of lidocaine or ketamine.
Condition or Disease
- Laparoscopic Bariatric Surgery
Phase
Study Design
Study type: | INTERVENTIONAL |
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Status: | Active, not recruiting |
Study results: | No Results Available |
Age: | 18 Years and older (Adult, Older Adult) |
Enrollment: | 87 (ESTIMATED) |
Funded by: | Other |
Allocation: | Randomized |
Primary Purpose: | Treatment |
MaskingQUADRUPLE:
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Clinical Trial Dates
Start date: | Apr 01, 2021 | ACTUAL |
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Primary Completion: | Jun 30, 2023 | ESTIMATED |
Completion Date: | Jul 30, 2023 | ESTIMATED |
Study First Posted: | Aug 24, 2020 | ACTUAL |
Results First Posted: | Aug 31, 2020 | |
Last Updated: | Apr 08, 2022 |
Sponsors / Collaborators
Intravenous lidocaine is widely used to reduce postoperative pain and to reduce perioperative opioid as a multimodal analgesia. From Cochrane review, perioperative lidocaine can decrease pain at rest, postoperative ileus and postoperative nausea and vomiting in elective and urgent surgery. Few trials in obese patients underwent laparoscopic bariatric surgery found that lidocaine infusion can decrease opioid consumption. However, the supported evidence is still limit. Ketamine has been used for postoperative analgesia as well, as an effective adjunct to decrease opioid consumption in various types of surgery, including open bariatric surgery. Moreover, the recent retrospective study (Tovikkai P, in press) found that there was a positive interaction between intraoperative lidocaine infusion and ketamine for decreasing opioid consumption in obese patients underwent laparoscopic bariatric surgery. However, the benefit of lidocaine and ketamine for postoperative pain in obese patients underwent laparoscopic bariatric surgery is still debated.
Therefore, we designed this study to examine the effect of intraoperative lidocaine infusion and intraoperative lidocaine infusion combined with intraoperative low-dose ketamine infusion on opioid consumption in obese patients undergoing laparoscopic bariatric surgery.
Participant Groups
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Participants in this arm will receive intra-operative lidocaine and ketamine infusion as adjunctive drugs for pain control. All medication is dosed based on calculated lean body weight (LBW) by Janmahasatian formula.
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Participants in this arm will receive only intra-operative ketamine infusion as adjunctive drugs for pain control. All medication is dosed based on calculated lean body weight (LBW) by Janmahasatian formula.
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Participants in this arm will receive normal saline, same volume as lidocaine and ketamine.
Eligibility Criteria
Sex: | All |
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Minimum Age: | 18 |
Age Groups: | Adult / Older Adult |
Healthy Volunteers: | Yes |
1. Adults patients age older than 18 years.
2. Body mass index more than 30 kg/m2.
3. Scheduled for laparoscopic bariatric surgery, including laparoscopic sleeve gastrectomy, robotic-assisted laparoscopic sleeve gastrectomy, laparoscopic Roux-en-Y gastric bypass surgery or robotic-assisted laparoscopic gastric bypass.
Exclusion Criteria:
1. Patient refusal.
2. Inability to communicate or read in Thai language.
3. Allergic to lidocaine or ketamine.
4. History of opioid use within 2 weeks before surgery
5. Cardiovascular disorder, including high grade atrioventricular block (second degree or third degree), history of coronary artery disease, poor controlled hypertension.
6. History of stroke, intracranial hemorrhage or intracranial mass
7. Cognitive impairment
8. Schizophrenia or history of antipsychotic drugs
9. Pregnant or breast-feeding patients
10. Conversion to open surgery
Primary Outcomes
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post-extubation cough graded by care giver using modified Minogue scales, which defined grade1 as no coughing or muscular stiffness, grade 2 as coughing once or twice, or transient cough response to removal of tracheal tube that resolved with extubation, grade 3 as ≤ 3 coughs lasting 1-2 seconds, or total duration of coughing last ≤ 5 seconds and grade 4 as ≥ 4 coughs with each lasting \> 2 seconds, total duration of coughing last \> 5 seconds.
Secondary Outcomes
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time since incision started until the last suture done recorded in minutes.
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time since anesthetic started until finished and patient out of room recorded in minutes.
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time since admission until discharge recorded in hours.
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cardiac arrhythmia, myocardial infarction, respiratory compromised, reintubation, readmission.
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sore throat score grading by self-assessment score, which defined grade 0 as no sore throat, grade 1 as minimal sore throat, grade 2 as moderate sore throat and grade 3 as severe sore throat.
More Details
NCT Number: | NCT04524130 |
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Other IDs: | 610/2563(IRB3) |
Study URL: | https://clinicaltrials.gov/study/NCT04524130 |