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NCT05212272 · ClinicalTrials.gov registry record · NA

MRI in High-Grade Glioma Patients Undergoing Chemoradiation

A NA study of High Grade Glioma, sponsored by Wake Forest University Health Sciences.

Recruiting
Registry status
NA
Development phase
16
Enrollment target
1
Study location

NCT05212272 is a NA study of High Grade Glioma that is actively recruiting participants, run by Wake Forest University Health Sciences. The registered enrollment target is 16 participants, below the 65-participant average among 42 other High Grade Glioma trials with a reported enrollment target (75% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT05212272, a NA study of High Grade Glioma, is actively recruiting participants, sponsored by Wake Forest University Health Sciences.

RECRUITING
Registry status
NA
Development phase
16 participants
Enrollment target
1
Study location

Study Summary

The purpose of this research study is to see if investigators can predict how brain functioning changes after radiation treatment based on PET scans and blood tests. Most participants experience at least mild decreases in their memory or attention after radiation therapy. Investigators hope that PET scans, lumbar puncture, and blood tests might help investigators predict who might have larger changes in their brain function after radiation.

Conditions Studied

Interventions

  • PROCEDURE PET-MRI Brain Scan
  • DIAGNOSTIC_TEST Blood draw
  • BEHAVIORAL Memory testing
  • PROCEDURE Optional lumbar puncture for cerebrospinal fluid collection

Study Locations (1)

North Carolina

  • Wake Forest Baptist Comprehensive Cancer Center - Winston-Salem

Trial Details

FieldValue
Enrollment Target 16 participants
Start Date 2022-09-02
Est. Completion 2026-12
Phase NA

Sponsor

Wake Forest University Health Sciences

1,140 total trials

What the Registry Record Tells You About NCT05212272

The ClinicalTrials.gov registry entry for NCT05212272 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 16 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 65-participant average among 42 other High Grade Glioma trials with a reported enrollment target (75% lower). The listed sponsor is Wake Forest University Health Sciences, which has 1,140 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with High Grade Glioma appearing as the primary indexed condition, and to 4 interventions - of which PET-MRI Brain Scan is the first listed.

NCT05212272 reports 1 study location spanning 1 distinct geographic area - top geographies include North Carolina.

Frequently Asked Questions

What is clinical trial NCT05212272 about?

NCT05212272 is a clinical study titled "MRI in High-Grade Glioma Patients Undergoing Chemoradiation". The purpose of this research study is to see if investigators can predict how brain functioning changes after radiation treatment based on PET scans and blood tests. Most participants experience at least mild decreases in their memory or attention after radiation therapy. Investigators hope that PET...

What is the current status of trial NCT05212272?

This trial is currently recruiting. It is a NA study. The enrollment target is 16 participants. The study started on 2022-09-02. Estimated completion is 2026-12.

What conditions does trial NCT05212272 study?

This clinical trial studies the following conditions: High Grade Glioma.

What interventions are being tested in trial NCT05212272?

The interventions under investigation include: PET-MRI Brain Scan (PROCEDURE), Blood draw (DIAGNOSTIC_TEST), Memory testing (BEHAVIORAL), Optional lumbar puncture for cerebrospinal fluid collection (PROCEDURE).

Who is sponsoring clinical trial NCT05212272?

This trial is sponsored by Wake Forest University Health Sciences, which has 1,140 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05212272 being conducted?

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

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

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