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临床试验/NCT06546475
NCT06546475尚未招募4 期

Tapering Antipsychotics in Patients With Remitted Psychosis: From Bedside to Bench Employing Animal Model and N-Acetylcysteine Study and Back to Bedside

National Taiwan University Hospital0 个研究点目标入组 20 人开始时间: 2024年8月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
尚未招募
入组人数
20
主要终点
Relapse rate (%)

研究概览

简要总结

The investigators are going to observe if add-on of n-acetylcysteine (NAC) 1200 or 2400 mg/d during tapering of antipsychotics in patients with remitted psychosis can help to reduce the pre-requisite of stabilization to 3 months (compared to the 6 months prerequisite of a previous Guided Antipsychotic Reduction to Minimum Effective Dose (GARMED) trial,) smoothly, without increased risk of relapse or frequency of adverse events compared to the 2-year results of the GARMED trial

详细描述

Trial procedure

  • Pretreatment: more instructions were delivered regarding the extent and the tempo of dose reduction, warning signal of relapse, timing to call for help if in need to resume rescue dose, and a shared decision-making process during tapering. Pre-treatment of NAC 1200 mg/d will be given for 1-2 weeks and then titrated up to 2400 mg/d to test tolerability. Patients will stay at either dose throughout the remaining of the course as preferable.
  • Dose tapering schedule: In the beginning, no more than one-quarter of the baseline antipsychotic dose will be reduced at a time. Patients need to be monitored every 4 weeks (or 1 month) by phone or in person. If they can maintain stabilized for 12 weeks (or 3 months) in a reduced dose, they can take next tapering of no more than one quarter of their current dose again, yielding 9/16 (3/4x3/4) of baseline dose. The subsequent dose reduction will be a reiteration of the previous step, cutting off one-quarter of the current dose following the formula (3/4) powered by n, rather than cutting off another 1/4 of the initial dose. The processes will be reiterated for 4 steps for one year.
  • Conditions during tapering: Noteworthily, when the patient is eligible to consider next dose reduction, he or she is empowered to take shared decision-making as they might opt to stay at their current dose for a more extended time for any reason. Patients can reach the study team during the course whenever they felt unsure if any relapse sign might be re-emerging. As needed use of benzodiazepines or hypnotics will be allowed to help control suspected signs of relapse. Patients will be supervised to stay at current dose for a longer term or even re-escalate to previous higher dose if any sign of suspected relapse re-emerges, and then will be closely monitored if their symptoms can be stabilized within 2 weeks.
  • Defining relapse: If a patient's recurrent psychotic symptoms cannot be controlled (any PANSS score > 3 in P1, P2, P3, G5, or G9) within 2 weeks under an antipsychotic dose equal to their baseline dose, the patient will be designated as having a relapse.
  • Practicability of dosing: The actual dose taken would not always be precisely the number calculated by the formula (3/4)n, as it was impractical to cut off a quarter or even smaller piece of a tablet for daily dosing. Several versions of intermittent or irregular dosing schedules have been generated to meet the needs.
  • Extent of dose reduction: The percentage of doses reduced at a designated time point will be calculated by the following formula: [1- (current dose)/(baseline dose)]x100%.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Both male and female outpatients or patients at psychiatric daycare service
  • Age 18-60 years old at the time of screening
  • A diagnosis of schizophrenia, schizophreniform disorder, psychosis NOS, based on the DSM-5 criteria
  • With a Positive and Negative Syndrome Scale (PANSS), score < 3 in all 3 positive symptoms (P1: delusion, P2: conceptual disorganization, P3: hallucination) and 2 general symptoms (G9: unusual thought, G5: mannerism and posturing) for at least 3 months
  • With a PANSS score < 4 in all 3 negative symptoms (N1: blunted affect, N4: social withdrawal, N6: lack of spontaneity/flow in conversation) for at least 3 months
  • Currently receiving antipsychotic treatment at a fixed dose for at least 3 months, including long-acting injectable antipsychotic
  • No revised use of benzodiazepines, antidepressants, anticholinergics, or other concomitant medications during the past 3 months

排除标准

  • A score of 5 or more on any of the 30 PANSS rating items at screening
  • Admission to the acute psychiatric unit during the past 6 months
  • A change in dose of current antipsychotic medication in recent 3 months
  • Concomitant use of mood stabilizers, such as lithium, valproic acid, or other anti-epileptic drugs
  • Mental retardation known as IQ below 70 prior to the diagnosis of schizophrenia
  • A history of pervasive mental disorder or bipolar disorder
  • A medical condition with significant cognitive sequelae
  • A history of substance dependence during the past 6 months
  • Currently in pregnancy or breastfeeding
  • A history of allergy to N-Acetylcysteine
  • Patient with phenylketonuria ( because the Actein Effervescent Tablet 600 mg/tab contains aspartame)

研究组 & 干预措施

NAC add-on 1

Experimental

NAC add-on with 1200 mg/d

干预措施: N-Acetylcysteine (Drug)

NAC add-on 2

Active Comparator

NAC add-on with 2400 mg/d

干预措施: N-Acetylcysteine (Drug)

结局指标

主要结局

Relapse rate (%)

时间窗: 1 year

If a patient's recurrent psychotic symptoms cannot be controlled (any PANSS score \> 3 in P1, P2, P3, G5, or G9) within 2 weeks under an antipsychotic dose equal to their baseline dose, the patient will be designated as having a relapse

次要结局

  • Self-report of Quality of Life(1 year)
  • Clinical severity: symptoms(1 year)
  • Clinical severity: global(1 year)
  • Extent of dose reduction (%)(1 year)
  • Personal and Social Functioning(1 year)
  • Self-report of subjective wellbeing(1 year)

研究者

申办方类型
Other
责任方
Sponsor

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