跳至主要内容
临床试验/NCT03632044
NCT03632044进行中(未招募)4 期

Evaluation of Trigeminal Nerve Blockade in the Pterygopalatine Fossa for Cleft Palate Repair: a Pilot Study

University of Florida2 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2018年11月20日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
进行中(未招募)
入组人数
40
试验地点
2
主要终点
Change in time to oral intake following palatoplasty for cleft palate

研究概览

简要总结

Cleft palate repair requires high doses of opioids for pain control postop. An alternative approach is placement of nerve blocks in the pterygopalatine fossa bilaterally, blocking the maxillary nerve & covering the entire midface. Application of bilateral suprazygomatic maxillary nerve blockade of the infraorbital nerve may provide effective analgesia for cleft lip repair, improving time to oral intake, pain control and time to hospital discharge.

详细描述

Cleft palate is a common congenital anomaly for which surgical repair is indicated during early childhood. The surgical repair of cleft palate is very painful, and generally requires high doses of opioids for adequate pain control, placing children at risk for post-operative respiratory depression and airway obstruction. An alternative approach to post-operative analgesia for cleft palate repair is the placement of nerve blocks in the pterygopalatine fossa bilaterally, blocking the maxillary nerve and covering the entire mid-face. This randomized, double-blinded study will investigate the utility of maxillary nerve blockade in controlling post-operative pain, decreasing opioid requirements, improving post-operative oral food and drink intake, and decreasing hospital length-of-stay after cleft palate repair.

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
Triple (Participant, Care Provider, Outcomes Assessor)

盲法说明

During the block placement the surgical team will be asked to leave the operating room briefly to remain blinded to the group assignment of all patients as the surgical team will manage the subjects post-operative care and determine discharge readiness.

ICU nursing staff and parents will be informed of participation in the study but will not be informed as to group assignment to remain blinded.

入排标准

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

入选标准

  • Patient presenting for palatoplasty for cleft palate only.
  • Parent/guardian consents to participate
  • Normal oral food and water intake before surgery
  • No underlying chronic pain condition

排除标准

  • Parent/guardian refuses to consent
  • Patient requires revision surgery on the palate
  • Patient requires surgery in addition to palatoplasty, including, but not limited to pharyngeal flap or soft palate lengthening procedures.
  • Any underlying chronic pain condition
  • Presence of any other factor which, at the discretion of any member of the study team, makes the patient a poor candidate for block placement.
  • Presence of any other factor which, at the discretion of any member of the study team, makes the patient a poor candidate for research participation.
  • History of Pierre Robin sequence
  • Planned or anticipated need for any type of artificial airway post-op

研究组 & 干预措施

25 Gauge needle

Sham Comparator

Subcutaneous placement of a 25 Gauge needle as a sham comparator after the induction of general anesthesia. Nothing will be injected.

干预措施: Sham Comparator (Other)

Suprazygomatic maxillary nerve blockade

Experimental

A single injection into the pterygopalatine fossa bilaterally of 0.2% ropivacaine at a dose of 0.15 mL/kg (block) after the induction of general anesthesia.

干预措施: Ropivacaine (Drug)

结局指标

主要结局

Change in time to oral intake following palatoplasty for cleft palate

时间窗: Change from baseline (post-op) and through study completion, an average of 96 hours.

Application of bilateral suprazygomatic maxillary nerve blockade of the infraorbital nerve to provide effective analgesia for cleft lip repair, improving time to oral intake after surgery.

次要结局

  • Change in amount of opioids following palatoplasty for cleft palate(Change from baseline (post-op) and through study completion, an average of 96 hours.)
  • Change in length of hospitalization following palatoplasty for cleft palate(Change from baseline (post-op) and through study completion, an average of 96 hours.)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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