Community Academic Profiles

Garry Gold

MRI Imaging of the Human Larynx

Contact Information

Stanford University School of Medicine 300 Pasteur Drive Stanford, CA 94305

Primary Contact:

Edward Damrose (650) 725-6500
To view all clinical trials at Stanford, please see the Clinical Trials Directory.

Brief

To determine if high resolution MRI can detect early invasion of cartilage by laryngeal carcinoma, and to determine if high resolution MRI may be superior to conventional MRI imaging or CT imaging to detect cartilage invasion.

Recruiting Status:

Recruiting

Stanford Recruiting Status:

Recruiting

Condition(s):

Intervention(s):

  • Procedure: High resolution MRI scan of the larynx using a custom-designed surface coil

Phase:

N/A

Eligibility

Ages Eligible for Study:

18 years to Any Age

Genders Eligible for Study:

Male and Female

Health of Volunteers:

People with the conditions listed in this trial can participate as controls.

Key Inclusion Criteria:

- Patients with benign or malignant neoplasm of the larynx.

- Patients who have undergone prior surgery, radiation therapy, or chemotherapy for cancer of the laryngopharynx will be eligible to participate.

- Patients 18 years of age and older at time of evaluation, male and female, all ethnicities.

- Ability to understand and the willingness to sign a written informed consent document.

Key Exclusion Criteria:

- Pregnancy

- Claustrophobia.

- Anatomic parameters which preclude scanning, such as limited range of neck motion, or inability to remain flat for at least 15 minutes.

- Patients with implanted devices (eg, defibrillator, pacemaker) that are a known contraindication to magnetic resononance imaging.

- Allergy to gadolinium contrast.

Additional Study Details

Official Title:

High Resolution MRI in the Evaluation of Laryngeal Neoplasia

Anticipated start date:

7/1/2009

Lead Sponsor:

Stanford University

Investigator(s):

Study Type:

Interventional

Purpose:

Treatment

Allocation:

Non-randomized

Masking:

Open

Control:

none

Assignment:

Single Group

Endpoints:

Safety/Efficacy

Primary Outcomes:

  • Tumor stage as determined by HRMRI.
  • Tumor stage as determined by histopathology in excised larynges.
  • Estimate the precision of HRMRI in terms of cartilage invasion.
  • Estimate the precision of HRMRI in discriminating between edema and tumor in patients with prior radiotherapy or chemotherapy.

Total Number to be Enrolled:

20

Total Number to be Enrolled at Stanford:

20

More Information

Trial Unique Id: SU-05292009-2661

Secondary ID(s):

  • 96536
  • ENT0019

Locations & Contacts

Stanford Locations & Contacts:

Stanford University School of Medicine 300 Pasteur Drive Stanford, CA 94305

Primary Contact:

Edward Damrose (650) 725-6500

Non-Stanford Locations:

The Stanford website does not have any locations outside of Stanford listed for this trial. You may want to check clinicaltrials.gov for posible additional locations.

This listing was last updated:

8/18/2009

PLEASE NOTE:

Study Coordinators and Research Nurses cannot give medical advice over the phone. Telephone numbers are provided for obtaining additional information on specific clinical research trials only. If you have specific questions which require clinical expertise, please call your primary care physician. If you do not have a primary care physician please feel free to call the SHC Physician Referral Service at (800) 756-9000 or send an email.

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