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临床试验/IRCT20210831052351N1
IRCT20210831052351N1招募中3 期

Evaluation of efficacy of celecoxib as add on to risperidone to reduce positive , negative and cognitive symptoms in schizophrenic patients in active phase: a double-blind, randomized and placebo-controlled clinical trial

niversity of social welfare and rehabilitation sciences0 个研究点目标入组 52 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
招募中
发起方
入组人数
52

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 years 至 65 years(—)
性别
All

入选标准

  • Patients with schizophrenia in the acute phase
  • Age range 18 to 65 years
  • Receiving only one Antipsychotic drug (Risperidone)
  • IQ greater than 70
  • Having the consent of the patient and his / her guardian to participate in the research

排除标准

  • Having a debilitating physical illness
  • patients with depression
  • Received an electric shock in the last two weeks
  • History of gastric ulcer or acute gastric bleeding
  • Pregnancy and lactation
  • No extra pyramidal symptoms in the study entry based on Simpson-Angus scale
  • Drug, alcohol or drug abuse in the last 6 months (excluding nicotine)
  • There is another diagnosis based on DSM5, including mood disorders and mental retardation
  • Blindness and deafness

研究者

发起方
niversity of social welfare and rehabilitation sciences

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