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

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02711215
Enrollment
80
Registered
2016-03-17
Start date
2015-05-31
Completion date
2020-01-31
Last updated
2019-09-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Major Depressive Disorder

Brief summary

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.

Interventions

DIAGNOSTIC_TESTPET/MR [11C]DASB

2 PET/MR scans will be performed (placebo/citalopram - double-blind randomized cross-over)

DRUGCitalopram

8mg citalopram or placebo (saline) will be applied during PET/MR measurements in a double-blind randomized cross-over design

DRUGEscitalopram (Mirtazapine/Duloxetine/Venlafaxine)

After completion of imaging procedures, patients will receive treatment with escitalopram 10-20mg. In case of non-response, after 6 weeks, treatment will be switched to either Mirtazapine, Duloxetine or Venlafaxine

DRUGPlacebo

8mg citalopram or placebo (saline) will be applied during PET/MR measurements in a double-blind randomized cross-over design

Sponsors

Medical University of Vienna
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
Yes

Inclusion criteria

* 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

Exclusion criteria

* 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

Design outcomes

Primary

MeasureTime frame
Hamilton Depression Scale (HDRS)12 weeks

Countries

Austria

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 16, 2026