跳至主要内容
临床试验/CTRI/2021/09/036952
CTRI/2021/09/036952进行中(未招募)4 期

To Compare the therapeutic efficacy of Scopolamine versus Ketamine in Treatment Resistant Depression

GMC Patiala0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
4 期
状态
进行中(未招募)
发起方

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

入选标准

  • Primary diagnosis of MDD without psychotic features based on DSM-5.
  • Fulfilling TRD (Thase and Rush) criteria, stage II: Failure of at least 2 adequate trials of at least 2 distinctly different classes of anti-depressants.
  • Ability to remain on adequate stable antidepressant regimen (on & off label treatment) for >4 weeks.
  • Medically stable for study participation.
  • Subject will be off the drugs that are likely to interact with glutamate for at least 14 days before the start of study.
  • Participants who will give voluntary informed consent.

排除标准

  • ââ?¬Â¢History of chronic psychosis or drug induced psychosis of any kind.
  • ââ?¬Â¢Currently, DSM-5 diagnosis of drug abuse/dependence in the last six months and has a negative drug screen at baseline.
  • ââ?¬Â¢Women will be excluded if they are pregnant, lactating or neither surgically-sterile nor using appropriate methods of birth control. Women must agree to continue using applicable birth control throughout the trial. All women of child-bearing potential must have a negative urine pregnancy test.
  • ââ?¬Â¢History of seizures, renal insufficiency or congestive heart failure.
  • ââ?¬Â¢History of clinically significant violence.
  • ââ?¬Â¢History of ketamine abuse/dependence or prior clinically significant adverse reaction to ketamine.
  • ââ?¬Â¢Current alcohol abuse or dependence.
  • ââ?¬Â¢Untreated hypertension (Systolic B.P >130mmHg and/or Diastolic B.P >80mmHg).
  • ââ?¬Â¢Clinically, abnormal liver function tests (LFTs), thyroid, renal function or anemia

研究者

发起方
GMC Patiala

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