跳至主要内容
临床试验/NCT02495220
NCT02495220Unknown2 期

Subtenon Versus Intravenous Dexmedetomidine for Postoperative Analgesia and Vomiting Control in Infantile Cataract Surgery

Assiut University1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2015年7月最近更新:
适应症
干预措施

试验速览

阶段
2 期
入组人数
80
试验地点
1
主要终点
postoperative CRIES pain scale score

研究概览

简要总结

The purpose of the present study was to evaluate the efficacy and safety of subtenon block (SB)anesthesia with dexmedetomidine in combination with bupivacaine versus intravenous dexmedetomidine for postoperative analgesia and emesis control in infants undergoing cataract surgery.

详细描述

In this prospective, randomized, controlled, double blind trial eighty ASA physical status grade I and II infants (1-12month) undergoing elective cataract surgery in one eye under general anesthesia were studied. Infants were randomly allocated to one of the two groups: subtenon block Group (SB) with dexmedetomidine (n =40) or intravenous dexmedetomidine Group (IV) (n =40). After securing the airway, infants in Group (SB) received SB block with 0.05 mL/kg of 0.5%bupivacaine and 0.5µ/kg dexmedetomidine mixture, whereas infants in Group (IV) received 1µ/kg IV dexmedetomidine after induction of anesthesia. Surgery started after 5 min of study drug administration. Postoperative assessment for number of infants requiring rescue analgesia and rescue antiemetics was the primary outcome. CRIES pain scale score , vomiting scale score during4-h study period, incidence of oculocardiac reflex and any surgical difficulty were the Secondary outcomes.

研究设计

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

入排标准

年龄范围
1 Month 至 12 Months(Child)
性别
All
接受健康志愿者

入选标准

  • ASA physical status grade I and II infants (1-12month).
  • undergoing elective cataract surgery in one eye under general anesthesia.

排除标准

  • infection of the orbit,
  • increased intraocular pressure(IOP),
  • history of allergy to local anesthetics,
  • history of previous eye surgery,
  • cardiovascular or clotting disorders,
  • full stomach,inner ear disorders or other conditions predisposing to vomiting
  • airway abnormalities
  • compromised sclera.

研究组 & 干预措施

subtenon block Group (SB)

Experimental

received SB block with 0.05 mL/kg of 0.5%bupivacaine and 0.5µ/kg dexmedetomidine mixture

干预措施: SB dexmedetomidine bupivacaine block (Drug)

intravenous dexmedetomidine Group(IV)

Experimental

received 1µ/kg IV dexmedetomidine after induction of anesthesia

干预措施: intravenous dexmedetomidine (Drug)

结局指标

主要结局

postoperative CRIES pain scale score

时间窗: 4 hours postoperatively

(0-2 for each parameter)

Postoperative assessment for number of infants requiring rescue analgesia and rescue antiemetics

时间窗: 4 hours postoperatively

by analysis for number of infants withCRIES pain scale score \>3

次要结局

  • Number of oculocardiac reflex(OCR)events(acute reduction in heart rate of >20%).(intraoperative period)
  • vomiting scale score(4 hours postoperative)

研究者

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

jehan ahmed sayed

assistant professor in anesthesia and intensive care department,faculty of medicine assiut university

Assiut University

研究点 (1)

Loading locations...

相似试验