UnknownNot Applicable

Magnetic Resonance Flow Measurements of Mesenteric Arteries and Veins and Portal Vein

Netherlands62 participantsStarted 2016-08

Plain-language summary

To determine the difference in baseline MR flow measurements and post-prandial MR flow measurements between patients diagnosed with CGI and patients not diagnosed with CGI.

Who can participate

Age range18 Years

SexALL

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Inclusion criteria

✓. Patients suspected of CGI referred to our hospital for further analysis
✓. Age ≥ 18 years
✓. Patients who gave informed consent

Exclusion criteria

✕. Age \< 18 years
✕. Unable to give informed consent
✕. Pregnancy
✕. Contra-indications for MRI: a. Metal implants which cannot be removed. E.g. cardiac pacemakers/ICD, aneurysm clips, metal stents, artificial heart valve, cochlea/retinal implants, hearing aids, dentures with magnetic click system or with other metal accessories, tattoos with metallic dye, metal plates/pins/screws of bones, piercings b. Claustrophobia c. Inability to lie still for 1 hour to 1,5 hours
✕. Other criteria the physician considers are not compatible with this study

What they're measuring

Determination of difference in baseline MR flow measurements and post prandial MR flow

Timeframe: 2.5 years

Trial details

NCT IDNCT02875600

SponsorErasmus Medical Center

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2021-12

Contact for this trial

Laurens Groenendijk

31 10 7033612 l.groenendijk@erasmusmc.nl

View on ClinicalTrials.gov More Ischemia trials