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Clinical Trials/CTRI/2015/06/005935
CTRI/2015/06/005935
Recruiting
未知

Comparative study of efficacy and safety of botulinum toxin A injections and suction curettage in the treatment of axillary hyperhidrosis

Indian Academy of Dermatology Venereology and Leprosy0 sites20 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Health Condition 1: null- Axillary hyperhidrosis
Sponsor
Indian Academy of Dermatology Venereology and Leprosy
Enrollment
20
Status
Recruiting
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional

Investigators

Sponsor
Indian Academy of Dermatology Venereology and Leprosy

Eligibility Criteria

Inclusion Criteria

  • 18 to 75 years
  • Persistent bilateral primary axillary hyperhidrosis
  • Gravimetrically minimal 50 mg spontaneous sweat production in each axilla, measured during 5 minutes in room temperature in calm condition
  • signed informed consent

Exclusion Criteria

  • Medical condition that can be dangerous by treatment with Botulinum toxin, including myastenia gravis, Lambert\-Eaton syndrome and each other disease that can interfere with the neuromuscular function
  • Secondary hyperhidrosis
  • Known allergy against study medication
  • Use of aminoglycosides, curare\-like products, or other products which can interfere with the neuromuscular function

Outcomes

Primary Outcomes

Not specified

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