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Clinical Evaluation of a Laser Heated, Fiberoptic-Coupled Radiation Dose Verification System


Phase 1
N/A
N/A
Not Enrolling
Both
Neoplasm

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Trial Information

Clinical Evaluation of a Laser Heated, Fiberoptic-Coupled Radiation Dose Verification System


We propose to determine the response of a newly developed laser heated, vycor glass
fiberoptic radiation dosimetry system to ionizing radiation in a clinical radiotherapy
environment. Present systems measure only total dose or have limitations, such as
instability, non-linearity, excessive size or a decoupled measurement system, making them
unsuitable in a variety of clinical applications. This fiberoptic coupled dosimetry system
is a new and innovative technology application which allows on-line measurement of
instantaneous dose rate and total dose never before achievable. It offers a clear advantage
in patient treatment delivery, allowing on-line corrections essential to a new generation of
radiotherapy treatment machines with development of beam intensity modulation as an adjunct
to 3D conformal therapy. It also has the advantage of submillimeter size and is minimally
invasive, making it ideal for brachytherapy.

This system has the potential for stable, accurate, reproducible, clinically feasible
measurements of total dose and dose rate. The output of this system will be measured under
various clinical conditions encountered in a clinical setting and compared against existing
thermolumeniscent and diode dosimetry standards. Initial measurements will use a tissue
equivalent phantom for depth dose and accuracy measurements. Additional studies will
include dosimetric measurements of routine clinical treatment setups on patients receiving
therapeutic irradiation.

Inclusion Criteria


INCLUSION CRITERIA:

Patients receiving either external beam radiotherapy or a radioactive implant under
established primary clinical protocols at the NCI or the National Naval Medical Center.

Patients must be willing to have the additional measurements performed and sign an
informed consent.

EXCLUSION CRITERIA:

Pediatric and cognitively impaired subjects will not be eligible for this study.

Type of Study:

Interventional

Study Design:

Endpoint Classification: Safety Study, Primary Purpose: Treatment

Authority:

United States: Federal Government

Study ID:

970129

NCT ID:

NCT00026871

Start Date:

July 1997

Completion Date:

May 2006

Related Keywords:

  • Neoplasm
  • Non-Therapeutic
  • Radiation Therapy
  • Dosimetry
  • Dose-Rate
  • Fiberoptic
  • Neoplasms

Name

Location

National Cancer Institute (NCI) Bethesda, Maryland  20892