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NCT05054998 · ClinicalTrials.gov registry record · Phase 4

Dual Time Point FDG PET/MRI Scan in Improving the Imaging Cancer Patients With Brain Metastases

A Phase 4 study, sponsored by M.D. Anderson Cancer Center.

Completed
Registry status
Phase 4
Development phase
12
Enrollment target

NCT05054998: Completed Phase 4 study, sponsored by M.D. Anderson Cancer Center.

NCT05054998 is a Phase 4 study that has completed, run by M.D. Anderson Cancer Center. The registered enrollment target is 12 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05054998, a Phase 4 study, has completed, sponsored by M.D. Anderson Cancer Center.

COMPLETED
Registry status
Phase 4
Development phase
12 participants
Enrollment target

Study Summary

This phase IV trial studies how well delaying positron emission tomography (PET)/magnetic resonance imaging (MRI) scan after injection of fluorodeoxyglucose (FDG) can improve the imaging of patients with cancer that has spread to brain (brain metastases). FDG is a type of imaging agent that doctors use to help "see" the images on a scan more clearly. Delaying PET/MRI scan after injecting FDG may improve how well doctors can tell the difference between healthy and unhealthy tissue.

Interventions

  • PROCEDURE Magnetic Resonance Imaging
  • PROCEDURE Positron Emission Tomography
  • RADIATION Fludeoxyglucose F-18

Trial Details

FieldValue
Enrollment Target 12 participants
Start Date 2018-08-03
Est. Completion 2024-04-26
Phase Phase 4

Sponsor

M.D. Anderson Cancer Center

2,692 total trials

What the Registry Record Tells You About NCT05054998

The ClinicalTrials.gov registry entry for NCT05054998 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 12 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is M.D. Anderson Cancer Center, which has 2,692 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 3 interventions - of which Magnetic Resonance Imaging is the first listed.

NCT05054998 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT05054998 about?

NCT05054998 is a clinical study titled "Dual Time Point FDG PET/MRI Scan in Improving the Imaging Cancer Patients With Brain Metastases". This phase IV trial studies how well delaying positron emission tomography (PET)/magnetic resonance imaging (MRI) scan after injection of fluorodeoxyglucose (FDG) can improve the imaging of patients with cancer that has spread to brain (brain metastases). FDG is a type of imaging agent that doctors ...

What is the current status of trial NCT05054998?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 12 participants. The study started on 2018-08-03. Estimated completion is 2024-04-26.

What interventions are being tested in trial NCT05054998?

The interventions under investigation include: Magnetic Resonance Imaging (PROCEDURE), Positron Emission Tomography (PROCEDURE), Fludeoxyglucose F-18 (RADIATION).

Who is sponsoring clinical trial NCT05054998?

This trial is sponsored by M.D. Anderson Cancer Center, which has 2,692 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, the data changelog, or report a data error.