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Real-time Assessment of Frameless Intrafraction Motion

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified September 2010 by Oregon Health and Science University.
Recruitment status was:  Active, not recruiting
Sponsor:
ClinicalTrials.gov Identifier:
NCT01202539
First Posted: September 16, 2010
Last Update Posted: September 16, 2010
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Oregon Health and Science University
  Purpose
The purpose of this study is to assess the ability of a modified thermoplastic mask system in keeping an individual head stationary for a predefined amount of time. The investigators hope to know if the modified mask is study enough, and also if the modification on the mask will allow the investigator see and track the individual's movement underneath the mask by means of a camera that can detect light reflected from the individual. Participants will lay down on their backs and their heads will be held in place with the mask system for approximately 1 hour.

Condition
Brain Tumor

Study Type: Observational
Study Design: Observational Model: Case-Only
Time Perspective: Prospective
Official Title: Use of Real-time Infrared Reflective Marker Tracking and Surface Texture Mapping to Assess the Integrity of a Novel Thermoplastic Mask System for Frameless Immobilization

Further study details as provided by Oregon Health and Science University:

Estimated Enrollment: 20
Study Start Date: September 2010
Estimated Study Completion Date: September 2011
Estimated Primary Completion Date: September 2011 (Final data collection date for primary outcome measure)
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
Potential subjects will be recruited by the Oregon Health and Science University study investigators.
Criteria

Inclusion Criteria:

  • Healthy individual
  • Age > 18 years.
  • Males and females of all races and ethnic groups

Exclusion Criteria:

  • Severe claustrophobia
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01202539


Locations
United States, Oregon
Oregon Health and Science University
Portland, Oregon, United States, 97239
Sponsors and Collaborators
Oregon Health and Science University
Investigators
Principal Investigator: James A. Tanyi, Ph.D. Oregon Health and Science University
  More Information

Additional Information:
Responsible Party: James A. Tanyi, PhD, Oregon Health & Science University
ClinicalTrials.gov Identifier: NCT01202539     History of Changes
Other Study ID Numbers: OHSU IRB00006460
First Submitted: September 15, 2010
First Posted: September 16, 2010
Last Update Posted: September 16, 2010
Last Verified: September 2010