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临床试验/NCT02512887
NCT02512887招募中不适用

Caudal vs Local Anesthesia in Hypospadias: The CLASH Study

McMaster University4 个研究点 分布在 1 个国家目标入组 224 人开始时间: 2016年7月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
招募中
入组人数
224
试验地点
4
主要终点
Recruitment rate

研究概览

简要总结

Hypospadias is one of the most common congenital malformations of the genitalia in boys, and is typically managed by surgical intervention. During pediatric urological surgery, caudal anesthesia is one of the most common regional anesthetic techniques used. Also known as caudal block, it has been shown to be a safe and effective anesthetic technique in children with a low incidence of anesthesia-related complications.While the reported incidence of complications directly associated with caudal block is low, there is scarce and inconclusive evidence on the impact of caudal anesthesia on the incidence of surgical complications. As a result, the objective of this superiority, randomized controlled trial is to assess whether the use of caudal anesthesia, when compared to dorsal penile block, is associated with a higher rate of urethrocutaneous fistulas and glans dehiscence post hypospadias repair.

详细描述

The rationale to conduct a definitive study comes as a result of the limitations inherent in the pre-existing literature due to selection bias, and the primarily retrospective nature of the current evidence, which is unclear whether caudal blocks result in higher complication rates following hypospadias repair. The only way to close this knowledge gap and disturb the current state of clinical equipoise surrounding this topic is to randomly assign the two interventions (caudal or penile block) to patients undergoing hypospadias repair. The rationale to conduct this pilot study is to determine whether the definitive study is feasible and to ensure that any methodological issues are identified and addressed prior to investing significant resources in a definitive trial.

This study will be a pilot study to determine the feasibility of conducting a large definitive superiority, parallel, randomized controlled trial (RCT) to assess whether dorsal penile block results in fewer postoperative complications than caudal block in boys (6-48 mos.) undergoing hypospadias repair.

Hypospadias repair will be carried out under standardized analgesic administration.. Participants may be given fentanyl (1-3 mcg/kg) at the discretion of the anesthesiologist. Anesthesia will be delivered to all participants via inhalation induction with air/nitrous oxide and sevoflurane. In addition either caudal anesthetic block (0.25% bupivacaine 1 ml/kg to a maximum of 10 ml) or dorsal penile block (bupivacaine without epinephrine 10-20 ml/kg) will be administered based on our randomization scheme. Each patient will also receive antiemetic prophylaxis with dexamethasone 150 mcg/kg ondansetron 50 mcg/kg Acetaminophen suppository 40 mg/kg, and intravenous morphine (0.02-0.1 mg/kg).

At Home At home, Oral Morphine (0.2 mg/kg) q4h prn, Ditropan (0.2 mg/kg) q12h prn, Tylenol (15 mg/kg/dose) q4h or Ibuprofen (10 mg/kg/dose) q6h will be prescribed at discharge to be administered at the parents' discretion. Trimethoprim (2 mg/kg) will also be prescribed for administration until catheter removal.

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
Single (Outcomes Assessor)

入排标准

年龄范围
6 Months 至 48 Months(Child)
性别
Male
接受健康志愿者

入选标准

  • Males 6-48 months of age at presentation to Pediatric Urology clinics
  • Patient who requires hypospadias repair by fellowship-trained Pediatric Urologists.

排除标准

  • Patients who have undergone previous hypospadias surgery
  • Patients who have contraindications to either caudal or dorsal penile block
  • Inability of parent/guardian to understand English/French
  • Deviation to pre-established anesthesia protocol

研究组 & 干预措施

Caudal Block Anesthesia

Experimental

Anesthesia will be delivered via inhalation induction with air/nitrous oxide and sevoflurane, and injection of 0.25% bupivacaine 1mL/kg without epinephrine into the caudal canal, which is the sacral portion of the spinal canal.

干预措施: Caudal Block Anesthesia (Drug)

Dorsal Penile Block Anesthesia

Active Comparator

Anesthesia will be delivered via inhalation induction with air/nitrous oxide and sevoflurane, and injection of 0.25% bupivacaine without epinephrine into the dorsal portion of the penis.

干预措施: Dorsal Penile Block Anesthesia (Drug)

结局指标

主要结局

Recruitment rate

时间窗: trial duration 1 year

Percentage of eligible participants enrolled, Randomization rate (percentage of enrolled participants randomized)

Protocol violations or Adverse events

时间窗: trial duration 1 year

Frequency of protocol violations or adverse events related to the study intervention.

Post-operative Complication Rate

时间窗: Follow-up to assess the complications, specifically urethrocutaneous fistula (UCF) and glans dehiscence within 12 months post-surgery.

UCF is defined as an abnormal communication between the reconstructed urethra and the skin located between the original meatus and the tip of the penis.Glans dehiscence is considered as a complete separation of the glans wings with or without a band of skin between them.

次要结局

  • Operating Room (OR) time(Record duration of operative time (takes on average 30-45 minutes))
  • Complications directly related to caudal block(Complications will be measured at a clinic visit 48 hours after surgery.)
  • Complications directly related to dorsal penile block(Complications will be measured at a clinic visit 48 hours after surgery.)
  • Post-operative Pain(Measure at patient admission and discharge at 30 minute intervals.)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (4)

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