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临床试验/NCT04622813
NCT04622813已完成3 期

The Effect of Intraoperative Nefopam, Ketoprofen and Paracetamol Combination vs Ketoprofen and Paracetamol Combination on Postoperative Morphine Requirements After Laparoscopic Cholecystectomy: A Randomized, Controlled Trial

American University of Beirut Medical Center1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2021年4月8日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
90
试验地点
1
主要终点
Total morphine consumption in the post anesthesia care unit

研究概览

简要总结

The goal of this clinical trial is to evaluate the effect of the addition of nefopam to a multimodal analgesic regimen consisting of ketoprofen and paracetamol during sevoflurane- dexmedetomidine-based anesthesia on postoperative morphine requirements in patients undergoing laparoscopic cholecystectomy.

详细描述

Nefopam is a centrally-acting anti-nociceptive compound with supraspinal and spinal sites of action. It inhibits monoamine reuptake, modulates descending serotoninergic pain, and may also interact with a dopaminergic pathway. Because its mechanism of action is distinct from that of other analgesic opioids, nefopam may well have a role in analgesic protocols. The role of nefopam in multimodal analgesia has been extensively investigated in laparoscopic cholecystectomy. However, there is general agreement that more studies are needed to determine the ideal multimodal strategy. No previous study has investigated a combination regimen of the three most commonly prescribed non-opioid analgesics (NOA) (nefopam, ketoprofen, and paracetamol) vs ketoprofen and paracetamol combination during sevoflurane-dexmedetomidine based anesthesia on pain control after laparoscopic cholecystectomy.

The aim of our study is to compare a combination regimen of three NOA (nefopam, ketoprofen, and paracetamol) vs ketoprofen and paracetamol combination during sevoflurane-dexmedetomidine based anesthesia on pain control after laparoscopic cholecystectomy. We will try to demonstrate the benefit with the addition of a third NOA, which is the nefopam, to the double-drug regimen including ketoprofen and paracetamol. Our hypothesis is that this combination regimen of three NOA is associated with less postoperative pain, less opioid consumption, shorter length of post-anesthesia care unit (PACU) stay, and fewer opioid-related adverse effects and postoperative complications compared to the double-drug regimen of ketoprofen and paracetamol.

In this prospective randomized double-blind study, 90 patients aged 18 to 64 years, with American Society of Anesthesiologists (ASA) physical status I and II, will be randomly assigned using a computer-generated random number table to one of two treatment groups. Group A will receive sevoflurane-dexmedetomidine based anesthesia with ketoprofen and paracetamol for postoperative pain control, and group B will receive sevoflurane-dexmedetomidine based anesthesia with nefopam, ketoprofen, and paracetamol for postoperative pain control. The primary outcome measure of this study is total morphine consumption in PACU. Normally distributed data will be summarized as mean ± SD and non-normally distributed data will be summarized as median [interquartile range]. This study would have an impact on our current practice and may help find out the best multimodal analgesic strategy to control postoperative pain after laparoscopic cholecystectomy.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 64 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • ASA physical status I-II
  • Age between 18 and 64 years
  • Patients able to give consent

排除标准

  • ASA physical status III to V
  • History of chronic pain
  • Use of an opioid analgesic within 12 hours prior to surgery
  • Alcohol or drug abuse
  • Chronic opioid intake
  • Morbid obesity
  • Psychiatric disorder
  • Pregnancy or breast-feeding
  • Intolerance to NSAIDSs
  • Allergy or contraindication to nefopam (acute angle-closure glaucoma, epilepsy, coronary artery disease, prostate adenoma), to morphine or paracetamol (liver failure), to ketoprofen (increased risk of bleeding, stomach or intestinal ulcer, chronic kidney disease) or to dexmedetomidine (uncontrolled hypertension, heart block greater than first degree, or other clinically significant morbidities)

研究组 & 干预措施

Placebo group

Placebo Comparator

Patients received sevoflurane-dexmedetomidine-based anesthesia with saline, ketoprofen and paracetamol for postoperative pain control,

干预措施: saline infusion, ketoprofen, paracetamol (Drug)

Multimodal group

Experimental

patients received sevoflurane-dexmedetomidine-based anesthesia with nefopam, ketoprofen, and paracetamol for postoperative pain control.

干预措施: nefopam, ketoprofen, paracetamol (Drug)

结局指标

主要结局

Total morphine consumption in the post anesthesia care unit

时间窗: Throughout the patient's stay in the recovery room (average of 30 minutes after the surgery)

Total morphine doses consumed after the surgery during the post anesthesia care unit stay of the patient

次要结局

  • Tachycardia(Intraoperatively and in PACU)
  • Respiratory depression(Throughout the patient's stay in the recovery room (average of 30 minutes after the surgery))
  • Number of patients receiving morphine on the floor(Throughout the patient's stay on the floor)
  • Total fentanyl(Intraoperatively)
  • Total morphine consumption at 24 hours after surgery(24 hours after surgery)
  • Quality of recovery(At 24 hours after the surgery)
  • Ketoprofen consumption(Throughout the patient's stay on the floor)
  • Paracetamol consumption(Throughout the patient's stay on the floor)
  • Number of patients receiving ketoprofen on the floor(On the floor)
  • Number of patients receiving paracetamol on the floor(On the floor)
  • Total morphine(Throughout the patient's stay on the floor)
  • NRS pain scores at rest in PACU(Throughout the patient's stay in the recovery room (average of 30 minutes after the surgery))
  • sedation scores in PACU(Throughout the patient's stay in the recovery room (average of 30 minutes after the surgery))
  • Time to first morphine requirement(From the time of arrival to PACU until discharge)
  • Time to discharge (readiness) from PACU(Throughout the patient's stay in the recovery room (average of 30 minutes after the surgery))
  • Nausea and vomiting(Throughout the patient's stay in the recovery room (average of 30 minutes after the surgery))
  • Pruritus(Throughout the patient's stay in the recovery room (average of 30 minutes after the surgery))
  • Overall satisfaction score(One month after surgery.)
  • Number of patients receiving morphine in PACU(Throughout the patient's stay in the recovery room (average of 30 minutes after the surgery))
  • Number of patients receiving morphine during the first 24 hours after surgery(During the first 24 hours after surgery)
  • NRS pain scores at 24 h after surgery(24 hours after surgery)
  • Rescue antiemetics(Throughout the patient's stay in the recovery room (average of 30 minutes after the surgery))
  • Urinary retention(Throughout the patient's stay in the recovery room (average of 30 minutes after the surgery))
  • Sweating(Intraoperatively and in PACU)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Sahar Sayyid

Professor

American University of Beirut Medical Center

研究点 (1)

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