Optimizing Contrast Dose and Scanning Parameters for Detection of Leptomeningeal Disease
Part of paid clinical trials in Houston, Texas.
- Sponsor
- M.D. Anderson Cancer Center
- Study ID
- NCT07415018
- Status
- Not Yet Recruiting
Notify me when recruiting opens
Save your spot on the interest list for this study. We'll keep your details with this study so our team can follow up when recruiting opens.
Add your contact details and location so we can keep your interest tied to this study.
Conditions
- Leptomeningeal Disease
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- MRI Scan — PROCEDUREGiven during standard of care
- VUEWAY — DRUGGiven by IV
- Gadavist — DRUGGiven by IV
Study Details
To learn if gadopiclenol (a contrast agent) used during MRI scanning can help in the detection of early LMD.
Key Dates
- Start date
- Jul 22, 2026
- Status verified
- Apr 2026
- Primary completion
- Jul 31, 2027
- Completion
- Jul 31, 2029
Study Design
- Enrollment
- 40 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- DIAGNOSTIC
Arms
- Other: MRI Scan with Gadavist (gadobutrol) / VUEWAY (gadopiclenol)Participants found to be eligible to take part in this study and agree to take part, will have brain MRI scans as part of standard of care. Then, within a week (preferably within 48 hours) of the participants routine brain MRI scans, you will have LMD-focused brain MRI scans with gadopiclenol contrast. Specifically, MRI scans will be done immediately after a small amount of gadopiclenol is given through an IV catheter placed into a vein, and then at 10 and 30 minutes thereafter. Then, a second dose of gadopiclenol will be given, and MRI scans will be done immediately after. The MRI scans performed for research purposes will take approximately 50 minutes to complete. You will be followed by routing clinical and imaging guidelines for 6 months or until the confirmation of LMD (whichever comes first).
Primary Outcome Measure
Safety and adverse events (AEs) [ Time Frame: Through study completion; an average of 1 year. ]
Central Contacts
- Rami Eldaya, MD(713) 745-2945
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| MD Anderson Cancer Center | Houston | Texas | 77030 | Rami Eldaya, MD (PRINCIPAL_INVESTIGATOR) |
Find similar trials in Houston, TX
By research site
Related Studies
- Standardized Clinical Assessment of Patients With Leptomeningeal MetastasisRecruiting · University of Zurich · Houston, Texas
- Prospective Evaluation Of High-Dose Systemic Methotrexate In Patients With Breast Cancer And Leptomeningeal MetastasisPHASE2 · Recruiting · Wake Forest University Health Sciences · Baltimore, Maryland
- B7-H3.CD28Z.CART in CNS NeoplasmsPHASE1 · Not Yet Recruiting · Robbie Majzner · Boston, Massachusetts