Dynamic Area Telethermometry (DAT) as an Imaging Modality in Patients With Cancer
1 other identifier
interventional
50
1 country
1
Brief Summary
The purpose of this study is to evaluate whether this new method of taking pictures called Dynamic Area Telethermometry (DAT) might be a good way of looking at patients with cancer that is relatively close to the surface of the body.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jan 2000
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2000
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 1, 2002
CompletedStudy Completion
Last participant's last visit for all outcomes
October 1, 2002
CompletedFirst Submitted
Initial submission to the registry
September 9, 2005
CompletedFirst Posted
Study publicly available on registry
September 14, 2005
CompletedDecember 28, 2007
December 1, 2007
2.8 years
September 9, 2005
December 20, 2007
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
To assess the feasibility of DAT in tumors detected by conventional imaging and evaluation of therapy induced changes in DAT imaging profile over time.
Interventions
Eligibility Criteria
You may qualify if:
- Histologically confirmed malignancy
- Primary or secondary tumor location amendable to DAT scanning: subcutaneous tissues
- Older than 15 years of age
- Able to withhold movement for 20 seconds, hold breath for 20 seconds for chest wall lesions and clinically stable acutely
You may not qualify if:
- Uncontrolled motion
- Tumors not verified or measurable by standard imaging
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Dana-Farber Cancer Institutelead
- Brigham and Women's Hospitalcollaborator
Study Sites (1)
Dana-Farber Cancer Institute
Boston, Massachusetts, 02115, United States
MeSH Terms
Conditions
Study Officials
- PRINCIPAL INVESTIGATOR
Milos Janicek, MD, PhD
Dana-Farber Cancer Institute
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- DIAGNOSTIC
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
September 9, 2005
First Posted
September 14, 2005
Study Start
January 1, 2000
Primary Completion
October 1, 2002
Study Completion
October 1, 2002
Last Updated
December 28, 2007
Record last verified: 2007-12