Validity of the Analgesia Nociception Index in Children and Adolescents With Chronic Pain
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 60
- 试验地点
- 1
- 主要终点
- Validation of analgesia nociception index (ANI) as a tool to assess change in the pain pressure threshold (PTT), measured by the PPT test, of children with chronic pain conditions.
研究概览
简要总结
The goal of this observational study is to learn about the analgesia nociceptive index (ANI) is associated with pain sensitivity in patients between the ages of 9-17 who are experiencing chronic pain. The main question it aims to answer is:
- Does the ANI score correlate with the change in the pain sensitivity in patients aged 9-17 undergoing an interventional block.
Patients already receiving an interventional block as part of their regular medical care for chronic pain will have their level of pain recorded during clinic appointments
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 9 Years 至 17 Years（Child）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Experiencing chronic pain defined by: persistent or recurrent pain at least once a week for at least three months in their electronic medical charts or by reference of the patient's physician
排除标准
- •Taking medications known to affect the sympathetic or parasympathetic nervous systems such as cholinomimetics (e.g., pilocarpine), anticholinergics (e.g., ipratropium), sympathomimetics (e.g., salbutamol), and adrenergic antagonists (e.g., propranolol).
- •Diagnosed cardiac or neurological conditions, including patients with arrhythmias, heart block, postural orthostatic tachycardia syndrome, Guillain-Barre syndrome, or spinal cord injury.
- •Active cancer diagnosis
- •Conditions that may interfere with the ability to understand instructions or complete assessments including: cognitive, or developmental delay.
- •Patients who do not speak English or French.
结局指标
主要结局
Validation of analgesia nociception index (ANI) as a tool to assess change in the pain pressure threshold (PTT), measured by the PPT test, of children with chronic pain conditions.
时间窗: 6 weeks
次要结局
未报告次要终点
研究者
Sabrina Carrie
Pediatric Anesthetist
McGill University Health Centre/Research Institute of the McGill University Health Centre