Thermal Signature of Patients Undergoing Radiation Therapy
Withdrawn before enrolling
Conditions studied: Lung Cancer
In brief
The goal of this clinical research study is to evaluate whether thermal imaging (recording body temperature) can be used to check the body's response to cancer therapy. Primary Objective: * The primary objective of this study is to establish techniques and methodologies of quantifying thermal signatures and their changes for cancer patients undergoing chemoradiation therapy. Secondary Objective: * The secondary objective is to evaluate correspondence between changes of thermal signature of a normal organ, e.g. lung or esophagus, versus the toxicity of that organ from chemoradiation therapy.
Key facts
- Study ID
- NCT00508313
- Run by
- M.D. Anderson Cancer Center
- People needed
- 0
- Starts
- 2007-07-01
- Expected to finish
- 2009-02-01
- Last updated by the study team
- 2016-04-08
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Patients with lung cancers of any stages.
- Patients will undergo chemotherapy or radiation therapy.
- Patients with KPS > 70, are physically mobile and independent, and are able to stand still straight for more than 10 minutes for imaging purposes.
- Age >18 years
You may not qualify if…
- Patients who had lung surgery within past 3 months.
- Patients with breast implant or cardiac implant (pace maker or defibrillator).
- Patients who had skin diseases (e.g. skin desquamation, dermatitis) or other medical conditions that may interfere with thermal measurement.
- Pregnant woman
- Extreme obese patients with body mass index >=35
Where it is running
- U.T.M.D. Anderson Cancer Center — Houston, Texas, United States
Full record on ClinicalTrials.gov
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