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A Prospective Comparative Study of a Novel Gadolinium-Weighted MRI Sequence Versus Conventional T1-Weighted Imaging for the Detection of Brain Metastases
Led by Region Stockholm · Updated on 2026-01-30
100
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating a new MRI technique called a gadolinium-weighted sequence to improve the detection of brain metastases in patients undergoing brain scans. The study aims to find out if this novel MRI method can identify more or smaller tumors compared to the standard T1-weighted imaging currently used. The goal is to enhance diagnostic accuracy without increasing the contrast dose or scan time. Participants will have a routine brain MRI with gadolinium contrast, followed by an additional scan using the new gadolinium-weighted MRI sequence during the same session. This new sequence includes advanced features to reduce background signals and better highlight tumors. Both imaging methods will be compared in the same exam to assess their ability to detect brain metastases. During the study, participants will undergo the combined MRI session lasting up to an hour after contrast injection. Researchers will measure the difference in the number of detected brain tumors between the two imaging sequences. The study involves patients known or suspected to have brain metastases and will monitor their ability to lie still during the exam and provide consent. The overall participation involves one MRI visit with no additional contrast or extended scan time.
CONDITIONS
Brief Title
Detection of Brain Metastases Using a Novel Gadolinium-Weighted MRI Sequence: A Prospective Comparison
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years or older
- Scheduled for clinical brain MRI with gadolinium contrast
- Known or suspected brain metastases
- Able to provide informed consent
- Able to lie still for the duration of the MRI examination
You will not qualify if you...
- Contraindications to MRI
- Known allergy or contraindication to gadolinium-based contrast agents
- Renal impairment (eGFR < 30 mL/min/1.73m²)
- Pregnant or breastfeeding
- Inability to comply with study procedures
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Single imaging session (within 1 hour of contrast administration)
Participants undergo a clinically indicated brain MRI with gadolinium contrast, receiving both the novel gadolinium-weighted MRI sequence and conventional T1-weighted imaging during the same scan session to compare lesion detection.
1 visit (in-person)
Trial Site Locations
Total: 1 location
1
Karolinska University Hospital
Stockholm, Solna, Sweden, 1171 76
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How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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