Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
NCT04118790

Microstructure Imaging in Stroke Patients

Led by Danish Research Centre for Magnetic Resonance · Updated on 2022-05-26

90

Participants Needed

2

Research Sites

479 weeks

Total Duration

On this page

Sponsors

D

Danish Research Centre for Magnetic Resonance

Lead Sponsor

B

Bispebjerg Hospital

Collaborating Sponsor

AI-Summary

What this Trial Is About

The purpose of this study is to establish a methodological framework based on existing advanced neuroimaging technologies as a new clinical neuroimaging tool for assessment of possible affected brain connections in stroke and TIA patients. Thus, providing new insights into microstructural changes that may underline why those patients experience deficits like fatigue.

CONDITIONS

Official Title

Microstructure Imaging in Stroke Patients

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with stroke or transient ischemic attack (TIA) with ABCD2 score greater than 4 and/or an acute Diffusion-Weighted Image (DWI) lesion
  • Modified Rankin Scale score of 2 or less
  • Ability to comply with all study requirements as determined by the investigator
  • Ability to understand and sign the informed consent form
  • Score of 12 or higher on the Multidimensional Fatigue Inventory for general fatigue
  • Healthy individuals age- and sex-matched to patient groups (for control group)
  • Ability to comply with all study requirements and understand and sign the informed consent form (for controls)
Not Eligible

You will not qualify if you...

  • General MRI research exclusion criteria defined by DRCMR
  • Pregnancy or breastfeeding; urine hCG test offered for women under 55 years
  • Major medical illnesses such as anemia, diabetes mellitus, thyroid disorders, cardiovascular disease, or electrolyte imbalance
  • Treatment with ritalin or modafinil
  • Known uncontrolled severe malignancy
  • Known drug or alcohol addiction
  • Fatigue caused by pharmaceutical side effects as identified by the investigator
  • Body weight over 130 kilograms
  • Persons unwilling to be informed about abnormal findings from study investigations
  • Recent infection within the last 3 weeks (for healthy controls only)
  • Known malignancy (for healthy controls only)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

Bispebjerg Hospital

Copenhagen, København NV, Denmark, 2400

Actively Recruiting

2

Danish Research Centre for Magnetic Resonance

Copenhagen, Denmark, 2650

Actively Recruiting

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Research Team

M

Maria del Carmen Moreno Genis, MSc

CONTACT

T

Tim Bjørn Dyrby, Professor

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

3

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