Abdominal Cancer Clinical Trial
— GCC0832Official title:
Investigating the Improvement in 4D CT Images Using Audiovisual Biofeedback: An Intra-fraction and an Inter-fraction Evaluation.
NCT number | NCT00780611 |
Other study ID # | HP-00043968 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | November 2008 |
Est. completion date | August 2011 |
Verified date | March 2020 |
Source | University of Maryland, Baltimore |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
This study will look at how tumors in the chest and abdomen move when you breathe. Your
doctors are studying if extra 4D CT scans and instructions on how to breathe can help predict
this type of movement and improve the accuracy of radiation treatment. 4D CT scans are
approved by the FDA. A 4D CT scan is different from a regular CT because it moves slower and
takes more pictures. It takes pictures of the way your body moves when you breathe. This
gives doctors more pictures of your body so that they can match your pictures to the way you
breathe.
In this study, instructions on how to breathe will be visual and audio. Visual instructions
will be given to you on a computer screen. You will hear audio instructions through a
speaker.
Status | Completed |
Enrollment | 25 |
Est. completion date | August 2011 |
Est. primary completion date | August 2011 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 86 Years |
Eligibility |
Inclusion Criteria: - Patients 18 years old or older - Patients undergoing a scan in the Department of Radiation Oncology for a thoracic or abdominal lesion(s) and identified as candidates for 4D CT. Exclusion Criteria: - Pregnant or breast-feeding women are excluded. - Negative serum or urine pregnancy test prior to study entry is required. Once on the protocol, the patient will be advised and expected to implement an accepted and effective method of contraception such as oral contraceptives ('the pill'),intrauterine devices (IUD's), contraceptive implants under skin or contraceptive injections and condoms with foam. - Patients who have difficulty lying flat on their back for extended periods of time will be excluded. |
Country | Name | City | State |
---|---|---|---|
United States | University of Maryland | Baltimore | Maryland |
Lead Sponsor | Collaborator |
---|---|
University of Maryland, Baltimore |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | To assess the efficacy of audio visual biofeedback for reducing artifacts for 4 -dimensional computer tomography (4DCT) | 8 scans over 3 days | ||
Secondary | To evaluate improvement in acquisition of a 4D CT by using audio-visual biofeedback including acquisition procedure, tumor quality | 8 scans over 3 days |
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