Expired Study
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Palo Alto, California 94306


Purpose:

Patients with excessive underarm odor and sweating and/or odor are treated with the VASER system to determine the VASER's effectiveness in reducing underarm sweat and odor


Study summary:

Patients with excessive underarm sweat and/or odor are recruited. The effect that excessive underarm sweat and/or odor has on their lifestyle is evaluated. They are surgically treated with the VASER system and followed up for 6 months to evaluate side effects, adverse events and effectiveness. Additional lifestyle evaluations are completed for comparison to pre-surgery answers.


Criteria:

Inclusion Criteria: - 18 years or older - Willing and able to appear for all scheduled, post-operative visits - Have axillary hyperhidrosis/bromidrosis that does not respond to conventional, non-invasive treatment Exclusion Criteria: - under the age of 18 - have undergone a prior surgical intervention for treatment of axillary hyperhidrosis (e.g.) Skoog procedure, ETS) - have been treated with a systemic or topical agent for axillary hyperhidrosis in the past 30 days - are deemed inappropriate candidates for surgery due to medical or mental health reasons - are currently being treated with investigational agents or have participated in an investigational study within 60 days prior to surgery - elect not to participate in the study


NCT ID:

NCT00735293


Primary Contact:

N/A


Backup Contact:

N/A


Location Contact:

Palo Alto, California 94306
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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