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OpenTrials
Completed

NCT Number: NCT01865604

Impact of tDCS on Cerebral Autoregulation

The aim of the study is to investigate whether there is a polarity-specific influence of tDCS on cerebral vasomotor reactivity monitored by transcranial doppler sonography.

Completed

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Key information

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • severe cerebral Microangiopathy
  • NOTCH3 carrier
  • Migraine with aura (IHS Classification ICHD-II)
  • Stenosis >80%, ECST-Criteria

Exclusion criteria

  • seizure disorder
  • history of severe alcohol or drug abuse, psychiatric illness like severe depression, poor motivational capacity
  • dementia

(1+2) history of stroke in past 3 months (3) migraine prophylaxis (4) contralateral stenosis >50%,

Treatment and study plan

Anodal tDCS

Device

Cathodal tDCS

Device

Sham tDCS

Device

Primary outcomes

  1. Cerebral vasomotor reactivity assessed by transcranial Dopplersonography

    Time frame: on 3 days within 12 weeks

    comparing cerebral vasomotor reactivity at baseline and after anodal/cathodal/sham stimulation

Sponsors and collaborators

Lead sponsor

Charite University, Berlin, Germany

Other

Registry information

Important dates

Study start
2012
Primary completion
2014
Study completion
2014
First posted
May 31, 2013
Registry last updated
Mar 16, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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