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NCT03052114Active, not recruiting

Electrical Impedance Tomography of Stroke and Brain Injury

Imaging Stroke, Epilepsy and Evoked Potentials in the Brain Using Electrical Impedance Tomography

Source: ClinicalTrials.gov · Last updated 1 Apr 2025

Brief summary (registry, in English)

The purpose of this study is to determine if Electrical Impedance Tomography (EIT) can produce reproducible and accurate images in people with stroke or head injury compared to existing standards such as MRI, CT. Electrical Impedance Tomography is a relatively new medical imaging method, which has the potential to provide novel images of brain function. It is fast, portable, safe and inexpensive, but currently has a relatively poor spatial resolution. It produces images of the internal electrical impedance of a subject with stroke or head injury using rings of ECG like electrodes on the skin. EIT recording will take place as early as possible, usually within 24 hours of admission. Following completion of the recording, the EIT images will subsequently be analysed and compared to other imaging data for accuracy.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
150 (estimated)
First submitted
9 Feb 2017
Start date
1 Oct 2015
Primary completion date
31 Dec 2027
Lead sponsor
University College, London
Diseases
Epilepsy, Stroke
NCT number
NCT03052114

What you commit to

  • Study type: Observational
  • Planned participants: 150
  • From 1 Oct 2015 to the primary completion date, 31 Dec 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • non (for stroke group)

Other

  • Any skull fractures or other injury which precludes the safe application of scalp electrodes (for head injury group)

Who the study is looking for

  • Patient with MRI or CT evidence of a stroke
  • Ability to give informed consent or have a consultee able to provide informed consent (for stroke group)
  • Any subject admitted for observation following a head injury (for head injury group)

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Hyper-Acute Stroke Unit University College Hospital
Coordinator of this site? Confirm its status
LondonUnited KingdomUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.