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Normal Brain Imaging Database for Brain Disorder Studies (Normal_tDCS)

U

University of Manitoba

Status

Active, not recruiting

Conditions

Healthy

Treatments

Device: transcranial direct current stimulation

Study type

Interventional

Funder types

Other

Identifiers

NCT03027869
B2016:074

Details and patient eligibility

About

Healthy volunteers will be recruited. All subjects will be tested a battery of neuropsychological tests, then undergo fluorodeoxyglucose-positron emission tomography (PET) and magnetic resonance imaging (MRI). During the PET and MRI, they will be stimulated with transcranial direct current stimulation (tDCS) for 15 minutes. A third of subjects will receive real tDCS on the left prefrontal cortex, a third on the right prefrontal cortex, and the other third will receive sham tDCS.

Enrollment

40 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • N/A

Exclusion criteria

  • History of any neurological or psychiatric diseases;
  • Abnormal MRI;
  • metal implants or a cardiac pacemaker;
  • Pregnant or breastfeeding women (female subjects of child bearing potential will be screened for pregnancy before MRI imaging).
  • severe hypertension.
  • cardiovascular disease.
  • Family history of epilepsy.

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

40 participants in 3 patient groups

Real Left DLPFC tDCS
Active Comparator group
Description:
Real tDCS on the left dorsolateral prefrontal cortex
Treatment:
Device: transcranial direct current stimulation
Sham tDCS
Sham Comparator group
Description:
30sec ramp-up and 30sec ramp-down
Treatment:
Device: transcranial direct current stimulation
Real Right DLPFC tDCS
Active Comparator group
Description:
Real tDCS on the right dorsolateral prefrontal cortex
Treatment:
Device: transcranial direct current stimulation

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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