Actively Recruiting

Age: 18Years +
All Genders
NCT07175077

7T Brain MRI Scan for Micro-brain Metastasis (microBM) Detection for Patients With Small-cell Lung Cancer (SCLC), Who Decline Prophylactic Cranial Irradiation (PCI)

Led by University of Missouri-Columbia · Updated on 2025-12-02

20

Participants Needed

1

Research Sites

95 weeks

Total Duration

On this page

Sponsors

U

University of Missouri-Columbia

Lead Sponsor

S

Siemens Medical Solutions

Collaborating Sponsor

AI-Summary

What this Trial Is About

Comparison of a 7t MRI to standard of care 1.5t/3t MRI scans to determine if earlier detection of brain metastases are possible on a 7t.

CONDITIONS

Official Title

7T Brain MRI Scan for Micro-brain Metastasis (microBM) Detection for Patients With Small-cell Lung Cancer (SCLC), Who Decline Prophylactic Cranial Irradiation (PCI)

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Histologically confirmed diagnosis of small-cell lung cancer (SCLC)
  • Brain MRI (1.5T or 3T) performed within 4 weeks prior to consent showing no brain metastases or leptomeningeal disease
  • No history of brain metastases or leptomeningeal disease
  • Refusal of prophylactic cranial irradiation (PCI) and agreement to surveillance with brain MRI scans (1.5T/3T)
  • Age 18 years or older
  • ECOG Performance Status of 0 to 2
  • Ability to tolerate the 7T MRI scan
Not Eligible

You will not qualify if you...

  • Contraindications to MRI such as implanted metal devices or foreign bodies
  • Contraindications to gadolinium contrast administration during MRI
  • Presence of other metastatic malignancies requiring active treatment
  • Pregnancy (pregnancy status will be confirmed verbally)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Missouri

Columbia, Missouri, United States, 65212

Actively Recruiting

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Research Team

B

Brooke McDaniel

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

0

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