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临床试验/NCT02711215
NCT02711215Unknown4 期

Patient Stratification and Treatment Response Prediction in Neuropharmacotherapy Using Hybrid Positron Emmission Tomography/Magnetic Resconance Imaging (PET/MR)

Medical University of Vienna2 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2015年5月最近更新:
适应症
相关药物

试验速览

阶段
4 期
入组人数
80
试验地点
2
主要终点
Hamilton Depression Scale (HDRS)

研究概览

简要总结

Selective serotonin reuptake inhibitors (SSRIs) raise serotonin (5-HT) in the synaptic cleft and are the current first line of pharmacological antidepressive treatment. Yet, there is a missing link between this first molecular step in their mechanism of action and observed clinical improvement. We have determined to establish a framework combining genuine molecular and functional imaging, i.e. hybrid pharmaco-PET/MR imaging, of the human serotonergic system in order to predict antidepressant treatment response.

Objectives:

  1. To predict antidepressant treatment response from data obtained using hybrid PET/MR with acute pharmacological challenge.
  2. To discriminate healthy from depressed subjects using this paradigm.
  3. To establish models connecting regional changes in occupancy of serotonin transporters (5-HTT) following citalopram infusion, with changes in brain activation and connectivity of major resting-state hub networks.

Design: Randomized, double-blind, placebo-controlled, cross-over mono-center study.

Materials and methods:

40 major depressed (MDD) and 40 healthy subjects will undergo 2 PET/MR scans on a 3T SIEMENS mMR Biograph scanner: 1. challenge with citalopram 8mg 2. placebo (saline). After structural imaging, functional MRI will be continuously acquired. [11C]DASB will be applied using a bolus + constant infusion paradigm to probe 5-HTT binding potentials and monitor 5-HTT occupancy with drug challenge, applied after 70min, in a single session. Scanning will be terminated 80min after challenge. MDD patients will receive subsequent escitalopram treatment with repeated evaluation of response for 3 months.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Basic Science
盲法
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 55 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • General health based on medical history, physical examination and structured clinical interview for DSM-IV (SCID)
  • HAM-D≥18 (patients)
  • Willingness and competence to sign the informed consent form
  • Age 18 to 55 years

排除标准

  • Any medical, psychiatric or neurological illness (other than MDD)
  • Current or former psychopharmacological treatment
  • Current or former substance abuse
  • Pregnancy
  • Any implant or stainless steel graft or any other contraindications for MRI
  • Failure to comply with the study protocol or to follow the instructions of the investigating team
  • Participation in studies involving radiation exposure in the past 10 years.
  • Body mass index <17 or >30

结局指标

主要结局

Hamilton Depression Scale (HDRS)

时间窗: 12 weeks

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Rupert Lanzenberger

Head of the Neuroimaging Labs

Medical University of Vienna

研究点 (2)

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