Investigational MRI Clinical Software and Hardware (Avery HS)

  • STATUS
    Recruiting
  • End date
    Jan 31, 2025
  • participants needed
    2000
  • sponsor
    Northwestern University
Updated on 24 March 2022
Accepts healthy volunteers

Summary

Patients and healthy volunteers will be scanned in order to test new sequences.

Description

The aims of this study are to:

  1. Conduct clinical protocol development and validation: The settings of an MRI machine are commonly adjusted according to the body part being scanned and the reason for the exam. When testing out new sequences and settings or adjusting existing settings, human subjects (patients and healthy volunteers) may be scanned in order to make sure that the quality of the images produced by the MRI machine is adequate for diagnostic purposes and to obtain normative values.
  2. Demonstrate and train: In some cases, human subjects may be scanned for the purposes of demonstrating equipment or for training operators on the safe and effective use of MRI systems.

Details
Condition Image, Body
Treatment MRI, Gadavist 2Ml Solution for Injection
Clinical Study IdentifierNCT05215132
SponsorNorthwestern University
Last Modified on24 March 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

• At least 18 years of age
Able to complete the MR safety questionnaire
Able to comprehend and provide informed consent in English
When contrast is being administered: healthy volunteers with a GFR≥60 ml/min
When contrast is being administered: patients with a GFR ≥30 ml/min

Exclusion Criteria

• When contrast is being administered: subjects with a GFR < 30 ml/min
When contrast is being administered: subjects with acute kidney injury
When contrast is administered, allergy to gadolinium-containing contrast media
Contraindication to MRI (implanted device, claustrophobia, dyspnea precluding the ability to follow breath-hold instructions)
Adults unable to consent
Individuals who are not yet adults
Pregnant or breastfeeding women
Prisoners
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How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer to help accelerate the development of new treatments and to get notified about similar trials.

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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