Expired Study
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San Francisco, California 94117


Purpose:

This is a safety and efficacy study of botulinum toxin type A in subjects with primary axillary hyperhidrosis.


Criteria:

Inclusion Criteria: - Primary axillary hyperhidrosis - Female or male, 18 years of age or older in good general health - Excessive sweating interferes with daily life activities and scores 3 or 4 on the HDSS at Screening and Baseline - Axillary sweat production of at least 50 mg/5 min measured gravimetrically Exclusion Criteria: - Any neurological condition, that may place the subject at increased risk with exposure to botulinum toxin type A such as amyotrophic lateral sclerosis and motor neuropathy, Lambert-Eaton syndrome, and Myasthenia gravis - Muscle weakness or paralysis, particularly in the upper extremities - Active skin disease or irritation or disrupted barrier at the treatment area - Undergone any procedures which may affect the axillary areas - Treatment with botulinum toxin type A in the axilla in the last 9 months or anywhere in the body in the last 6 months - Any prior axillary use of an anti-hyperhidrosis medical device - If menopausal had symptoms of menopause such as sweating or flushing within the last year


NCT ID:

NCT02565732


Primary Contact:

N/A


Backup Contact:

N/A


Location Contact:

San Francisco, California 94117
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: November 18, 2019

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