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临床试验/NCT05848505
NCT05848505已完成不适用

Effect of Preoperative Intranasal Dexmedetomidine on Fentanyl Requirements in Children Undergoing Tonsillectomy

Pierre-Yves P Lequeux1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2022年2月25日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
50
试验地点
1
主要终点
Perioperative fentanyl consumption

研究概览

简要总结

Background: Management of postoperative pain in paediatric patients undergoing tonsillectomy remains a challenge that faces anesthesiologists in their daily practice. High dose of opioids are usually necessary and are responsible for side effects like nausea, vomiting, constipation, delayed hospital discharge and more importantly respiratory depression and sleep apnea. Dexmedetomidine is a selective alpha two agonist that has an analgesic and anxiolytic effect with minimal effects on respiratory drive.

Goal of the study: The aim of this study is to assess the opioid sparing effect of preoperative intranasal dexmedetomidine as part of multimodal analgesia in the paediatric population undergoing tonsillectomy.

Methods: This will be a prospective, randomised, controlled, double blinded clinical trial with 50 participants who will be randomised between two groups: dexmedetomidine group and control group. The dexmedetomidine group will receive intranasal dexmedetomidine in the preoperative holding area while the other group will receive the placebo.

The primary endpoint will be the total fentanyl consumption in the perioperative period. Additionally, we will look at postoperative pain scores at 10, 30 and 60 minutes after recovery as well as the time to first opioid rescue analgesic and agitation scores as secondary endpoints. Blood pressure and hart rate will also be recorded throughout the study period.

详细描述

Tonsillectomy surgery is both common and painful in paediatric patients, usually requiring high doses of opioids, which are associated with many adverse effects. Dexmedetomidine is a sedative intravenous drug with analgesic and opioid-sparing effects but with side effects including (usually minor) bradycardia and hypotension which might delay hospital discharge. Intranasal dexmedetomidine, although off-label, has been extensively studied for its sedative effect as well as its safety profile and is associated with much less side effects (bradycardia and hypotension). It has however not being studied for its analgesic effects in children. The hypothesis is that preoperative intranasal dexmedetomidine will decrease total perioperative fentanyl consumption in children undergoing tonsillectomy.

Fifty ASA 1 or 2 patients aged from 3 yo to 6 yo scheduled for tonsillectomy (+/- adenoidectomy +/- myringotomy) will be included in this prospective, randomised, controlled, double blind trial and then randomised in two groups: dexmedetomidine group (DG) and control group(CG).

Exclusion criteria are: allergy to dexmedetomidine, paracetamol, ondansetron or dexamethasone, hepatic dysfunction, raised intracranial pressure or altered GCS or neuromuscular disease in addition to abnormal neurological development.

Upon arrival in the operating theater holding area, the patients will receive either 2mcg/kg of dexmedetomidine (DG) or the equivalent volume of normal saline (CG), both administered intranasally with a mucosal atomizer device attached to the syringe and equally distributed in both nostrils. Although intranasal dexmedetomidine is off-label, it is routinely administered as a premedication including in our institution. The syringes of dexmedetomidine and normal saline will be prepared by a nurse and both the patients and the anaesthetists will be blinded of the content of the syringes. The patients will then be moved to the operating room and a proper monitoring will be applied (ECG, pulse oximeter, non-invasive blood pressure and capnograph). Anaesthesia will be induced with inhalation of Sevoflurane without nitrous oxide and fentanyl 1 mcg/kg as well as a neuromuscular blocking agent (at the discretion of the anaesthetist) will all be administered as soon as an intravenous cannula is inserted. The trachea will then be intubated before the start of surgery. During the surgery, the anaesthetist in charge will give boluses of 1 mcg/kg of fentanyl when deemed necessary (tachycardia, hypertension, movements of the patient). All the patients will receive the usual analgesia regimen of SKMC consisting of paracetamol (15 mg/kg), dexamethasone (0.15 mg/kg) and ondansetron (0.1 mg/kg) before extubation.

In the Post-Anaesthesia Care Unit (PACU), the patients will be administered 0.5 mcg/kg of fentanyl q10min if their pain score (measured by the FLACC scale) is > 2/10 and repeated until the score is < 3. The PACU nurses will be blinded to which group the patients belong.

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
3 Years 至 16 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Patients undergoing elective tonsillectomy

排除标准

  • documented allergy to dexmedetomidine, paracetamol, ondansetron or dexamethasone
  • hepatic dysfunction
  • raised intracranial pressure or altered GCS
  • neuromuscular disease.

研究组 & 干预措施

Dexmedetomidine group

Experimental

Intranasal dexmedetomidine 2 mcg/kg administered before surgery

干预措施: Dexmedetomidine (Drug)

Control group

Placebo Comparator

Intranasal saline 0.02 mL/kg administered before surgery

干预措施: Dexmedetomidine (Drug)

结局指标

主要结局

Perioperative fentanyl consumption

时间窗: From induction of anesthesia to discharge of post-anesthesia care unit (expected less than 4 hours)

Cumulative perioperative (intraoperative and postoperative) fentanyl consumption

次要结局

  • Bradycardia(From induction of anesthesia to discharge of post-anesthesia care unit (expected less than 4 hours))
  • Postoperative sedation(From admission to discharge of post-anesthesia care unit (expected less than 3 hours))
  • Postoperative pain(From admission to discharge of post-anesthesia care unit (expected less than 3 hours))
  • Post-anesthesia care unit length of stay(From admission to discharge of post-anesthesia care unit (expected less than 3 hours))
  • Hypotension(From induction of anesthesia to discharge of post-anesthesia care unit (expected less than 4 hours))

研究者

发起方
Pierre-Yves P Lequeux
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Pierre-Yves P Lequeux

Consultant aneshesiologist

Sheikh Khalifa Medical City

研究点 (1)

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