跳至主要内容
临床试验/NCT05252650
NCT05252650Unknown不适用

Postoperative Pain Management in Pediatric Patients With Cerebral Palsy - Comparative Observational Study"

Biruni University1 个研究点 分布在 1 个国家目标入组 130 人开始时间: 2022年2月15日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
130
试验地点
1
主要终点
pain score

研究概览

简要总结

In this study, our aim is to examine orthopedic interventions, anesthesia method, postoperative pain level and management applied to patients with CP in biruni university hospital.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

入排标准

年龄范围
3 Years 至 15 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Diagnosed with cerebral palsy between the ages of 3-15,
  • Category 2 according to the Classification of the American Society of Anesthesiology (ASA 2),
  • patients undergoing soft tissue release for knee or ankle flexion contracture of the lower extremity with palliative or reconstructive hip interventions

排除标准

  • Any child with CP younger than 3 years old and older than 15 years has undergone
  • procedures without a specific diagnosis of CP,
  • the need for bone surgery,
  • requiring both hip, knee and ankle surgery in the same session,
  • with autonomic neuropathy,
  • Patients with a history of anticholinergic and vasoactive drug use or allergy to amide type local anesthetics

结局指标

主要结局

pain score

时间窗: 6 month

pain score with r-FLACC

次要结局

未报告次要终点

研究者

发起方
Biruni University
申办方类型
Other
责任方
Principal Investigator
主要研究者

ILKE KUPELI

investigator

Biruni University

研究点 (1)

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