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临床试验/NCT04766684
NCT04766684已完成4 期

A Randomized Comparison of Local Anesthetic Options for Clubfoot Tenotomy: Needle-Free Jet Injection Versus Topical Cream

Vanderbilt University Medical Center1 个研究点 分布在 1 个国家目标入组 107 人开始时间: 2021年6月1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
已完成
入组人数
107
试验地点
1
主要终点
FLACC (Face, Legs, Activity, Cry, Consolability) Scale

研究概览

简要总结

Infants undergoing Ponseti treatment for idiopathic clubfoot often require percutaneous tendoachilles lengthening (TAL) after serial casting. This procedure is frequently performed in the office with a local anesthetic to avoid exposure to general anesthesia in the operating room. Topical anesthetic creams are commonly used to provide local analgesia for this procedure. The cream is applied to the infant's skin around the achilles tendon and requires 30 minutes to provide adequate analgesia, reaching a depth of up to 5 mm at maximum effect. An alternative is a needle-free jet injection system that uses compressed CO2 to push 0.25 ml of lidocaine into the skin, providing local analgesia at the site of administration. This method likewise provides analgesia to the site of application at a depth of 5-8 mm, yet only takes approximately 1-2 minutes to achieve maximum effect.

Aim 1: Determine which pain management method, topical anesthetic cream (4% liposomal lidocaine) vs. jet infection of local anesthesia (1% lidocaine), provides the greatest pain relief to infants with clubfoot undergoing an in-office percutaneous TAL.

Hypothesis: Jet injection will provide equal or greater pain control when compared topical anesthetic cream.

Aim 2: Determine if there is a difference in the rate of adverse events between the two pain management methods, topical anesthetic cream (4% liposomal lidocaine) vs. jet infection of local anesthesia (1% lidocaine).

Hypothesis: Jet injection of local anesthesia will not be associated with an increased rate of adverse events in comparison to topical anesthetic cream.

If jet injection of local anesthesia is shown to provide comparable or better pain control without an increase in adverse events, use of this needle-free injection system will decrease the overall length of the procedure visit, thus increasing quality, safety, and value.

详细描述

Clubfoot is a common congenital birth deformity, with a prevalence of approximately 1 in 1000 live births. Without treatment, clubfoot can cause significant disability. Percutaneous tendoachilles lengthening (TAL) is commonly required to correct residual equinus deformity during the Ponseti method. TAL may be performed in the operating room under general anesthesia or in outpatient settings using local anesthesia, but evidence guiding optimal anesthetic strategies for in office procedures remains limited.

Effective pain control in infancy is critical. Experimental and clinical studies demonstrate that repeated early life painful stimuli lead to hyperinnervation, heightened sensitivity, altered stress responses, and lower pain thresholds later in life. Cumulative procedural pain is associated with poorer cognitive and developmental outcomes and early interventions to reduce pain lessen cortisol exposure and improve neurobehavioral trajectories. Poorly controlled pain during neonatal or early childhood procedures has also been linked to altered pain behaviors during later procedures, emphasizing the long lasting impact of early nociceptive experiences.

Existing approaches for in office TAL include needle infiltration of local anesthetic or application of topical anesthetic cream. Needle infiltration may create soft tissue swelling that obscures the tenotomy site and increases procedural difficulty, and both techniques have been associated with substantial infant distress despite adequate application.

Needle free jet injection offers a potential alternative. Prior studies demonstrate that jet injection produces less pain than conventional needle infiltration and provides superior analgesia to topical anesthetics for procedures such as venipuncture, intravenous catheter placement, and lumbar puncture.

The Clubfoot Tenotomy Trial (ClubTT) was designed to evaluate whether jet injected local anesthesia provides equivalent analgesic efficacy without increasing adverse events compared with topical anesthesia for infants with idiopathic clubfoot undergoing in office TAL.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

盲法说明

On the day of or after the final casting visit, the participant will be randomized in equal proportion (1:1) to either the control group (4% liposomal lidocaine cream with saline jet injection) or the intervention group (placebo cream with 1% lidocaine jet injection). Participants, care providers, investigators, and outcome assessors will be blinded to the randomization groups.

An outside pharmacy, the Health & Wellness Compounding Pharmacy, will provide and blind the 4% liposomal lidocaine and placebo creams. The Vanderbilt Investigational Drug Service will provide the blinded 1% lidocaine and saline vials for jet injection. The Investigational Drug Service will store the creams provided by the outside pharmacy and the jet injection vials. They will assist in dispensing the creams/vials to the outpatient clinic.

入排标准

年龄范围
— 至 6 Weeks(Child)
性别
All
接受健康志愿者
否

入选标准

  • •Clubfoot patients less than 6 weeks of age at start of casting
  • •Patients requiring in-office percutaneous achilles lengthening (TAL) following serial casting

排除标准

  • •Clubfoot patients greater than 6 weeks of age at the start of casting
  • •Previous clubfoot treatment
  • •Patients with a neuromuscular condition (spina bifida, caudal regression syndrome, arthrogryposis, etc.)
  • •In-office TAL is not recommended by treating physician

研究组 & 干预措施

Placebo cream and jet injection of 0.25mL 1% lidocaine

Experimental

干预措施: Jet injection of 1% lidocaine (Device)

4% liposomal lidocaine cream and jet injection of 0.25 ml saline

Active Comparator

干预措施: 4% liposomal lidocaine cream (Drug)

结局指标

主要结局

FLACC (Face, Legs, Activity, Cry, Consolability) Scale

时间窗: FLACC Score at the time of tenotomy (poke of the scalpel)

The FLACC scale is used to assess pain in children. For this study, it will be administered by the Certified Child Life Specialist. The Face, Legs, Activity, Cry, Consolability (FLACC) scale is a measurement used to assess pain in children between the ages of 2 months and 7 years or individuals that are unable to communicate their pain. The scale is scored in a range of 0-10 with 0 representing no pain. Lower values represent reduced pain on the scale

Heart Rate

时间窗: Heart Rate at the time of tenotomy (poke of the scalpel)

Heart Rate

Oxygen Saturation

时间窗: Oxygen saturation at the time of tenotomy (poke of the scalpel)

Pulse oximetry will be used to measure oxygen levels in the blood. An oxygen saturation level of 95 percent is considered normal

次要结局

未报告次要终点

研究者

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

Jeffrey Martus

Professor of Orthopaedic Surgery

Vanderbilt University Medical Center

研究点 (1)

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