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临床试验/NCT02407743
NCT02407743已完成不适用

Finding Good TEMporal PostOperative Pain Signatures (TEMPOS)

University of Florida1 个研究点 分布在 1 个国家目标入组 428 人开始时间: 2015年8月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
428
试验地点
1
主要终点
Measure postoperative pain scores change with respect to time

研究概览

简要总结

The purpose of this research study is to determine what causes pain after surgery to increase or decrease over time.

详细描述

Before surgery, study participants will be asked questions about age, gender, race/ethnicity, annual income, and education level. Study participants will also be questioned regarding prior pain experiences, their mood and how they think about pain. A small test tube of blood, a cheek swab or a saliva sample will be taken to see what genetic differences may influence individuals pain after surgery.

After surgery, study participants will be asked questions about their pain intensity while in the hospital. Additional information will be collected about the effects of pain medicine, and their recovery from surgery.

Following discharge from the hospital, study participants will be contacted monthly to confirm continued communication. Study participants will also be contacted six months after surgery, and asked to complete a final survey about their pain after surgery.

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
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 18 years of age or older
  • anticipated length of hospital stay of 72 hours or greater
  • expected post-operative survival greater than 6 months

排除标准

  • < 18 years of age
  • anticipated need for prolonged post-operative intubation (greater than 24 hours)
  • urgent or emergent surgical procedure
  • inability to understand or participate in questionnaires, surveys or data collection

结局指标

主要结局

Measure postoperative pain scores change with respect to time

时间窗: up to 7 days

Pain scores will be measured using previously established pain scale and Questionnaire

次要结局

  • Measure timing patterns that may influence development of persistent postsurgical pain (PPP)(up to 6 months)
  • Genetic testing(up to 1 day)
  • Measure variables that contribute to postoperative pain scores(up to 6 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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