Evaluation of Human Brain Tumor Therapy Response by Magnetic Resonance (MR)

NCT ID: NCT00724191

Last Updated: 2020-05-11

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

88 participants

Study Classification

OBSERVATIONAL

Study Start Date

1999-09-30

Study Completion Date

2014-01-15

Brief Summary

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The purpose of this study is to determine if new MRI methods that measure various information and chemical makeup in the brain, will give early information regarding response to treatment in patients with brain tumors.

Detailed Description

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The purpose of this study is to see if new MRI methods which measure information related to water, blood flow, and chemical makeup in the brain, can give early information of how well treatment is working in patients with brain tumors.

Conditions

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Brain Tumors

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Study Groups

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A

Evaluation of new MRI methods that measure information related to the chemical makeup of the brain in patients undergoing therapy for brain tumors.

MRI

Intervention Type PROCEDURE

New MRI methods which measure information related to water, blood, and chemical makeup in the brain.

Interventions

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MRI

New MRI methods which measure information related to water, blood, and chemical makeup in the brain.

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Patients over the age of 18 who have been diagnosed with a brain tumor of the central nervous system and a treatment plan has been discussed.
* Must be willing/able to undergo 3-5 MRI scans with IV contrast.
* You can take part in this study if you are NOT afraid of small, enclosed places.

Exclusion Criteria

* A patient who is claustrophobic.
* Females who are pregnant or lactating.
* Patients who have electrically, magnetically or mechanically activated implants such as heart pacemaker, magnetic surgical clips, prosthesis or or implanted neurological stimulator.
* Any patient who has a history of allergic reactions to MR contrast agent (Omniscan, Magnevist, MultiHance)
* Patients who require general anesthesia to complete MRI exam or patients who have had a negative reaction to MRI sedation. (Chloral Hydrate, Pentobarbital or Versed)
* You should NOT have any metals, or implanted devices in your body (such as aneurysm clips, pacemakers, or artificial joints or limbs.). You will need to tell us about your medical history including any surgeries you have had.

Also, if your job or any other experience might have left metal fragments in your body, please let us know, as the MRI has a strong magnetic field could move a metal fragment in your body or interfere with an implanted device, such as a pacemaker, causing you harm.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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National Institutes of Health (NIH)

NIH

Sponsor Role collaborator

National Cancer Institute (NCI)

NIH

Sponsor Role collaborator

University of Michigan

OTHER

Sponsor Role lead

Responsible Party

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Thomas L Chenevert, PhD

Primary Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Thomas L. Chenevert, Ph.D

Role: PRINCIPAL_INVESTIGATOR

University of Michigan

Locations

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Univeristy of Michigan Health System

Ann Arbor, Michigan, United States

Site Status

Countries

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United States

Other Identifiers

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5P01CA085878-12

Identifier Type: NIH

Identifier Source: secondary_id

View Link

CA85878-12

Identifier Type: OTHER_GRANT

Identifier Source: secondary_id

HUM 00051052

Identifier Type: -

Identifier Source: org_study_id

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