Expired Study
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New York, New York 10065


Purpose:

The purpose of this study is to demonstrate the safety of the AvicennaTM class IV laser for application over the skin of human subjects. In addition, we seek to measure the effectiveness and utility of this class 4 laser therapy in the treatment of post-thoracotomy pain syndrome.


Criteria:

Inclusion Criteria: - Men and women age 25-65 years old with chest wall pain after lung surgery lasting more than 2 months after surgery. - Subjects shall have failed conservative treatment which may include rest, physical therapy, braces, and over the counter anti-inflammatory medications. All those enrolled will be native English speakers and have at least a high school degree Exclusion Criteria: - Subjects will be excluded if they are pregnant (which will be confirmed by a urine pregnancy test if they are of childbearing age) - Have previous history of other pain syndromes or psychiatric disorders. - We will exclude the morbidly obese (BMI >30) because the laser may not be able to penetrate deep enough through adipose tissue. In addition, subjects who have had previous back surgery, or are on antidepressants for the treatment of depression in the preceding 6 weeks will be excluded as these may represent potential confounding factors.


NCT ID:

NCT00623909


Primary Contact:

Principal Investigator
Edward Rubin, MD
Weill Medical College of Cornell University


Backup Contact:

N/A


Location Contact:

New York, New York 10065
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: March 16, 2018

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