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临床试验/NCT03261921
NCT03261921已完成1 期

Adjuncts to Caudal Block in Pediatrics

Cairo University0 个研究点目标入组 63 人开始时间: 2016年6月5日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
63
主要终点
Time of first request of analgesia

研究概览

简要总结

One of the most commonly used regional anesthetic techniques in pediatric surgeries is the caudal epidural block. Its main disadvantage remains the short duration of action. Hence, different additives have been used. Dexmedetomidine as an additive to the local anesthetic bupivacaine in caudal epidural analgesia prolongs the duration of postoperative analgesia so is dexamethasone. The investigators aimed to study the effect of combining both additives in the duration of analgesia, decreasing side effects and decreasing anesthetic doses

详细描述

Sixty three children scheduled for hypospadias randomized into 3 groups. Group I (n=21) (dexamethasone 0.1mg/kg+ 0.5ml/kg bupivacaine 0.25%), group II(n=21)( dexmedetomidine 0.01ug/kg+ 0.5ml/kg bupivacaine 0.25%)and groupIII(n=21)(dexamethasone0.1mg/kg+dexmedetomidine0.01ug/kg +0.5ml/kg bupivacaine 0.25%).intraoperative and postoperative hemodynamics were recorded. In PACU, MOPS scores and sedation scores were recorded at 30min,1,2,3,6and 12hrs. Also the time of first analgesic request was recorded.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Factorial
主要目的
Diagnostic
盲法
Triple (Participant, Care Provider, Investigator)

盲法说明

The Patients allocated to study groups using computer generated random list & group assignment was sealed in sequentially numbered opaque envelopes that opened after induction of anesthesia.

入排标准

年龄范围
1 Year 至 6 Years(Child)
性别
Male
接受健康志愿者

入选标准

  • 1 - ASA I-II 2- Males only 3- Children aged from 1-6 years 4- Children scheduled for hypospadias surgery

排除标准

  • Contraindication to caudal anesthesia.
  • cardiovascular diseases.
  • drug allergy.
  • Type I diabetes.
  • Clotting disorders.
  • Mentally retarded children or those whose families did not approve inclusion in the study

研究组 & 干预措施

Dexamethasone group

Active Comparator

In this group the patients received 0.5 ml/kg of bupivacaine 0.25% + (0.1 mg/kg dexamethazone) caudally.

干预措施: Dexamethasone (Drug)

Dexamethasone group

Active Comparator

In this group the patients received 0.5 ml/kg of bupivacaine 0.25% + (0.1 mg/kg dexamethazone) caudally.

干预措施: Bupivacaine (Drug)

Dexmedetomidine group

Active Comparator

In this group the Patients received 0.5 ml/kg of bupivacaine 0.25% + dexmedetomidine(1 mu/kg) caudally.

干预措施: Dexmedetomidine (Drug)

Dexmedetomidine group

Active Comparator

In this group the Patients received 0.5 ml/kg of bupivacaine 0.25% + dexmedetomidine(1 mu/kg) caudally.

干预措施: Bupivacaine (Drug)

Combination group

Active Comparator

In this group the patients received 0.5 ml/kg of bupivacaine 0.25% + dexamethasone(0.1mg/kg) and dexmedetomidine (1 mu/kg) caudally.

干预措施: Dexamethasone (Drug)

Combination group

Active Comparator

In this group the patients received 0.5 ml/kg of bupivacaine 0.25% + dexamethasone(0.1mg/kg) and dexmedetomidine (1 mu/kg) caudally.

干预措施: Dexmedetomidine (Drug)

Combination group

Active Comparator

In this group the patients received 0.5 ml/kg of bupivacaine 0.25% + dexamethasone(0.1mg/kg) and dexmedetomidine (1 mu/kg) caudally.

干预措施: Bupivacaine (Drug)

结局指标

主要结局

Time of first request of analgesia

时间窗: 12 hours

the time from caudal block to the first time to analgesic needs

pain scores

时间窗: 12 hours

the modified objective pain score

次要结局

  • sedation score(12 hours)
  • heart rates(beat/minute)(3 hours.)
  • mean arterial pressure (mmhg)(3 hours)

研究者

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

Amany Hassan Saleh

principal investigator,MD of anesthesia and intensive care unit.

Cairo University

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