Actively Recruiting

Phase 1
Age: 18Years - 80Years
All Genders
Healthy Volunteers
NCT03705715

Identifying Correlates of Brain Microglial Activation in Neuropsychiatric Syndromes: a Dimensional Approach

Led by The University of Texas Health Science Center, Houston · Updated on 2025-03-19

200

Participants Needed

1

Research Sites

587 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The purpose of this research is to determine whether there is more extensive inflammation in the brain of people with clinical evidence of neuropsychiatric syndromes, such as mood disorder, chronic pain syndrome, dementia, traumatic brain injury, or substance abuse. The research will also explore whether there is more inflammation in patients with more neuropsychiatric symptoms. Inflammation in the brain will identified by using Positron Emission Tomography (PET) with the radiotracer \[11C\]PBR-28 or \[11C\]ER176.

CONDITIONS

Official Title

Identifying Correlates of Brain Microglial Activation in Neuropsychiatric Syndromes: a Dimensional Approach

Who Can Participate

Age: 18Years - 80Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Must be between 18-80 years old
  • Male or female
  • Must be right handed
  • Must be able to sit unaccompanied for long periods of time with little body movement
  • Must be illicit drug free at time of scanning as appropriate (negative urine drug screen)
  • Must be either healthy or have a diagnosis of a neuropsychiatric syndrome such as mood disorder, chronic pain syndrome, dementias, traumatic brain injury, or substance/alcohol use disorder
  • Healthy control volunteers must be medication free for at least 14 days
  • Illicit drug free at time of scanning (verified by negative urine drug screen)
Not Eligible

You will not qualify if you...

  • Must not be a smoker
  • Females must not be pregnant or nursing
  • Must not suffer from claustrophobia
  • Must not meet exclusion criteria for MRI scanning (e.g., presence of non-fixed magnetisable objects)
  • Must not be a PBR-28 low affinity binder (or using the [11C]ER176 radiotracer study)
  • Healthy control volunteers must not have ongoing, chronic, or relapsing/remitting medical, psychiatric, or neurological illness as determined by history, medical record, or examination

AI-Screening

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Trial Site Locations

Total: 1 location

1

BBSB at UTHealth

Houston, Texas, United States, 77054

Actively Recruiting

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Research Team

A

Alan Prossin, MBBS

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

BASIC_SCIENCE

Number of Arms

2

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