跳至主要内容
临床试验/CTRI/2020/04/024625
CTRI/2020/04/024625尚未招募未知

Preliminary assessment of the tolerability and efficacy of intermittent theta-burst magnetic stimulation (iTBS) on negative symptoms and cognitive functioning in schizophrenia

All India Institute of Medical Sciences New Delhi0 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
未知
状态
尚未招募
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

  • 1.Male or female right-handed individuals between 18 to 50 years of age meeting the DSM 5 criteria for schizophrenia (American Psychiatric Association, 2013)
  • 2.Illness duration of more than 2 years
  • 3.Patients currently stabilized on same antipsychotics for a period of at least 4 weeks but having significant negative symptoms (SANS scores >=60 and SAPS score <=50)
  • 4.Ability to read Hindi or English language
  • 5.Patients with capacity and willingness to give informed consent

排除标准

  • 1-Presence of any other psychiatric disorder or substance use
  • disorder (except caffeine or nicotine) through M.I.N.I 7.0. screening.
  • 2-History of seizure.
  • 3-History of receiving any treatment with brain stimulation.
  • 4- Known or suspected pregnancy or currently lactating.
  • 5-Presence of unstable medical illness.
  • 6-History suggestive of space occupying brain lesion or cerebro-vascular accident.
  • 7-Having implanted device or metal in brain/head or cardiac pacemaker or ferromagnetic dental braces.

研究者

发起方
All India Institute of Medical Sciences New Delhi

相似试验

进行中(未招募)
不适用
Preliminary evaluation of efficacy and tolerability of the association mesalazine 1g nifedipine 10mg in the treatment of tenesmus in patients suffering of distal ulcerative cholitis. Open study, phase II, two steps according to Simon - NDTenesmus in patients with distal ulcerative cholitisMedDRA version: 9.1Level: LLTClassification code 10038063Term: Rectal haemorrhage
EUCTR2006-003340-33-ITBRACCO
进行中(未招募)
1 期
Investigation of the effectiveness, tolerability and safety of ilon® Salbe classic in the treatment of acute inflammation of the hair follicleAcute folliculitis
EUCTR2016-005105-39-DECesra Arzneimittel GmbH & Co.KG130
进行中(未招募)
1 期
A Phase 1 Study to evaluate tolerability, safety and efficacy of AB122 and AB154 in Combination with Chemotherapy for Patients With Non-Small Cell Lung Cancer
JPRN-jRCT2051230009asermoaddeli Ali12
进行中(未招募)
不适用
An evaluation of the effectiveness and tolerability of tapentadol hydrochloride prolonged release, and tapentadol hydrochloride immediate release on demand, in subjects with uncontrolled severe chronic nociceptive, mixed or neuropathic low back pain taking either WHO Step I or Step II analgesics or no regular analgesics - NDlow back painMedDRA version: 12.0Level: LLTClassification code 10024891Term: Low back pain
EUCTR2009-010427-12-ITGrünenthal GmbH180
进行中(未招募)
不适用
An evaluation of the effectiveness and tolerability of tapentadol hydrochloride prolonged release, and tapentadol hydrochloride immediate release on demand, in subjects with uncontrolled severe chronic pain due to osteoarthritis of the knee taking either WHO Step I or Step II analgesics or no regular analgesics.Pain due to OsteoarthritisMedDRA version: 9.1Level: LLTClassification code 10031161Term: Osteoarthritis
EUCTR2009-010423-58-DEGrünenthal GmbH180