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
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