Expired Study
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Cleveland, Ohio 44195


Purpose:

The purpose of this study is to examine the effect of using a pulsed dye laser (the VBEAM), a non-ablative laser (the Affirm) and a combination of both lasers to improve the appearance of your surgical scar. Both the pulsed dye laser and Affirm laser are approved by the US Food and Drug Administration (FDA) for the treatment of scars. Surgical scars are a type of scar that can benefit from laser therapy. Redness and the appearance of small blood vessels near the surface of the skin (telangiectasias) develop in such scars as part of the normal healing process and usually spontaneously remit, but often slowly and incompletely. In many cases, lasers can accelerate the clearing of this redness and also improve scar texture.


Study summary:

In summary, we will perform a total of three laser treatments. A personal interview, clinical examination, and a photograph will be taken at each visit. At the end of the three treatments, a final personal interview, clinical evaluation and photograph will be taken to document the effects of the laser treatments. At the end of the study, the patient will have the option to receive two additional laser treatments four weeks apart, also at no cost, to the entire scar.


Criteria:

Inclusion Criteria: - Age 18 years and older - No significant medical illness - Surgical procedure that involves closure of the transverse abdominal incision performed in the department of dermatology and plastic surgery at the Cleveland Clinic main campus. - Subjects with the willingness and ability to understand and provide informed consent Exclusion Criteria: - Under 18 years of age - Pregnancy or Lactation - Subjects currently taking blood thinners or who have had chemotherapy or radiation within the last 6 months - Subjects with liver/kidney disease, diabetes mellitus, hypertension, connective tissue disease or who are immunocompromised - Subjects with a known susceptibility to keloid formation or hypertrophic scarring - Subjects who are unable to understand the protocol or to give informed consent - Subjects with mental illness - Subjects with obvious non-healing wound


NCT ID:

NCT00735254


Primary Contact:

Study Director
Rebecca Tung, MD
The Cleveland Clinic


Backup Contact:

N/A


Location Contact:

Cleveland, Ohio 44195
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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