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临床试验/NCT03110172
NCT03110172Unknown1 期

Short-term Efficacy of Antidepressant in Patients Underwent TKA

Dalian Municipal Central Hospital1 个研究点 分布在 1 个国家目标入组 32 人开始时间: 2017年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
发起方
入组人数
32
试验地点
1
主要终点
Pain score of participants with Duloxetine as assessed by Western Ontario and McMaster Universities Index after 4 weeks of treatment.

研究概览

简要总结

By taking certain antidepressant in early postoperative period,which is supposed to improve the psychological status of patients with osteoarthritis, explore the effect of certain antidepressant on the recovery of the early stage after the operation of knee joint replacement.

详细描述

In this study, the investigators are going to investigate the efficacy of Duloxetine on pain, physical function, mental health and quality of life in patients underwent TKAs.

The control group is going to be given celecoxib 200mg/24h to 2 weeks after operation.On the basis of the above scheme, the treatment group is going to receiving duloxetine 60mg/24h to 8 weeks after operation.HAMD-17 scale, KSS scale, SF-36 scale and WOMAC scale will be used to evaluate the two groups before and after operation for 4 and 8 weeks.

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
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
51 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • No extra articular malformations are diagnosed and accord with Kellgren-Lawrence criteria
  • Primary TKA surgery,Varus is smaller than 20°
  • Always there is no history of mental illness, no history of relevant medicine
  • Be able to read and understand Chinese, with good communication skills
  • Voluntary participation in this clinical study

排除标准

  • Previous history of mental and psychological illness
  • With severe diseases in respiratory system, circulatory system or digestive system
  • Allergic to duloxetine and celecoxib

研究组 & 干预措施

KSS scale

Active Comparator

Knee Society Score with Duloxetine Hydrochloride

干预措施: Duloxetine Hydrochloride (Drug)

HAMD-17 scale

Active Comparator

Hamilton Depression Score with Duloxetine Hydrochloride

干预措施: Duloxetine Hydrochloride (Drug)

SF-36 scale

Active Comparator

Medical Outcomes Study Short Form-36 score with Duloxetine Hydrochloride

干预措施: Duloxetine Hydrochloride (Drug)

WOMAC scale

Active Comparator

Western Ontario and McMaster Universities Index with Duloxetine Hydrochloride

干预措施: Duloxetine Hydrochloride (Drug)

结局指标

主要结局

Pain score of participants with Duloxetine as assessed by Western Ontario and McMaster Universities Index after 4 weeks of treatment.

时间窗: up to 6 months

A face-to-face questionnaire will be conducted by two trained interviewers

Function score of participants with Duloxetine as assessed by Knee Society Score after 4 weeks of treatment.

时间窗: up to 6 months

A face-to-face questionnaire will be conducted by two trained interviewers

次要结局

  • Pain score of participants with Duloxetine as assessed by Western Ontario and McMaster Universities Index after 8 weeks of treatment.(up to 6 months)
  • Function score of participants with Duloxetine as assessed by Knee Society Score after 8 weeks of treatment.(up to 6 months)

研究者

发起方
Dalian Municipal Central Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Zhu Bin

Principal Investigator,Graduate Student

Dalian Municipal Central Hospital

研究点 (1)

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