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RECRUITING

Measuring Brain Health Using Low-Field Portable MRI

NCT06533631 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to develop a new grading scale and utilize automated segmentation for measurement of White Matter Hyperintensity (WMH) volume using a low field MRI.

Interventions

  • DEVICE Portable low-field MRI (pMRI)
  • DEVICE 3T MRI

Study Locations (1)

Connecticut

  • Yale Magnetic Resonance Research Center (MRRC) at The Analyn Center (TAC) — New Haven

Trial Details

FieldValue
Enrollment Target 100 participants
Start Date 2025-02-05
Est. Completion 2026-11

Sponsor

Yale University

1,283 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06533631

The ClinicalTrials.gov registry entry for NCT06533631 describes a study currently listed as recruiting. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Yale University, which has 1,283 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with White Matter Hyperintensity appearing as the primary indexed condition, and to 2 interventions — of which Portable low-field MRI (pMRI) is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06533631 reports 1 study location spanning 1 distinct geographic area — top geographies include Connecticut. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06533631 about?

NCT06533631 is a clinical study titled "Measuring Brain Health Using Low-Field Portable MRI". The purpose of this study is to develop a new grading scale and utilize automated segmentation for measurement of White Matter Hyperintensity (WMH) volume using a low field MRI.

What is the current status of trial NCT06533631?

This trial is currently recruiting. The enrollment target is 100 participants. The study started on 2025-02-05. Estimated completion is 2026-11.

What conditions does trial NCT06533631 study?

This clinical trial studies the following conditions: White Matter Hyperintensity. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06533631?

The interventions under investigation include: Portable low-field MRI (pMRI) (DEVICE), 3T MRI (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06533631?

This trial is sponsored by Yale University, which has 1,283 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06533631 being conducted?

This trial has 1 study location across Connecticut. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial