跳至主要内容
临床试验/CTRI/2026/03/107153
CTRI/2026/03/107153尚未招募不适用

Lumateperone as an adjunctive therapy in negative and cognitive symptoms of Schizophrenia: An open label study

Central Institute Of Psychiatry, Ranchi1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2026年4月16日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
60
试验地点
1

研究概览

简要总结

Schizophrenia patients with negative and cognitive symptoms will be recruited and divided into 2 groups. one group will receive Tab Lumateperone 42mg OD for 4 weeks and will be clinically assessed using scales like BACS, and compared with baseline. Another group will receive usual treatment and compared with the other group.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
None

入排标准

年龄范围
18.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • participants satisfying the ICD-11 criteria for schizophrenia 2.illness duration of equal to or more than 2 years
  • patient giving written informed consent
  • score less than or equal to 25 in Hindi Montreal cognitive assessment test
  • PANSS negative symptoms score of equal to or more than 4 or more than 15 combined.
  • SANS score more than 20.

排除标准

  • Any other major comorbid psychiatric diagnosis or significant concurrent medical illness.
  • Patients with organic brain disorder and/or mental retardation.
  • Patients on treatment with medications that can influence cognitive functioning: Anticholinergics (except trihexyphenidyl).
  • Patients who have received ECT in the past 6 months.
  • Contraindications to use of Lumateperone.

研究者

发起方
Central Institute Of Psychiatry, Ranchi
申办方类型
Research institution and hospital
责任方
Principal Investigator
主要研究者

Dr Rishabh Nagar

Central Institute of Psychiatry

研究点 (1)

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