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临床试验/NCT00578136
NCT00578136已完成不适用

A Randomized-Double Blinded Trial Comparing the Analgesic Efficacy and Side Effects of Rectus Sheath Block vs. Infiltration of Surgical Site for Post Operative Pain Control After Umbilical Hernia Repair Surgery

Children's Hospital of Philadelphia1 个研究点 分布在 1 个国家目标入组 52 人开始时间: 2006年11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
已完成
入组人数
52
试验地点
1
主要终点
The Amount of Intravenous and Oral Opioids Used by Patients Who Receive a Rectus Sheath Nerve Block and Those Who Receive Local Infiltration of the Surgical Site for Postoperative Analgesia.

研究概览

简要总结

Umbilical hernia repair is a common painful outpatient procedure performed in children. Often analgesia for this procedure is provided by using local infiltration of the surgical site by the surgeons and perioperative opioids and NSAIDS both IV and orally. The use of opioids can cause adverse side effects which include, but are not limited to nausea, vomiting, itching, and respiratory depression, etc. The rectus sheath block can be performed in these patients to decrease their post operative pain.

详细描述

Umbilical hernia repair, a common Day Surgery procedure in children, is associated with considerable postoperative discomfort. The patient has to meet certain discharge criteria such as tolerating liquids, adequate level of analgesia, etc., prior to being discharged from the day surgery unit.

Currently, both rectus sheath block and local infiltration of the surgical site are used for providing post-operative analgesia for umbilical hernia repair surgery. The local infiltration can only be done at the end of the surgical procedure as it could alter the planes of the surgical field if performed preoperatively. We believe that the analgesia provided prior to the surgical incision will decrease the amount of intraoperative and postoperative opioids used and the subsequent side effects of these medications (5,6). The rectus sheath block, a regional anesthetic technique, offers possible improved pain management following umbilical hernia repair in a recent observational study (1-3,7). We will perform a double-blinded, randomized study to compare the efficacy of rectus sheath block and surgical infiltration in providing postoperative analgesia.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
5 Years 至 17 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Male or female subjects ages > 5 to < 18 years.
  • American Society of Anesthesiology (ASA)physical status 1 or
  • Patients who undergo an umbilical hernia repair at CHOP.

排除标准

  • Parents/patients refusal to the placement of a rectus sheath nerve block.
  • Subjects with allergy to bupivacaine.
  • Patients who are developmentally delayed which precludes their participation in pain scale reporting.
  • Parents who do not comprehend English sufficiently well to read the consent and ask questions.

研究组 & 干预措施

1

Active Comparator
  1. One group will receive the rectus sheath block prior to Umbilical hernia repair.

干预措施: Bupivacaine (Drug)

2

Active Comparator
  1. The second group will receive local anesthetic infiltration of the surgical site at the end the umbilical hernia repair.

干预措施: Bupivacaine (Drug)

结局指标

主要结局

The Amount of Intravenous and Oral Opioids Used by Patients Who Receive a Rectus Sheath Nerve Block and Those Who Receive Local Infiltration of the Surgical Site for Postoperative Analgesia.

时间窗: immediate to 24 hour post-operatively

total postoperative opioid and any additional analgesic medications.

次要结局

  • The Duration of Analgesia Based on Time to First Rescue Med, the Quality of Analgesia Based on Modified FACES Scale, and the Incidence of Side Effects: Nausea, Vomiting, Pruritus, and Assess Patient Satisfaction With Pain Management.(immediate to 24 hours post-operatively)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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