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A Randomized Clinical Trial Examining the Efficacy of Treatment of Cutaneous Verruca Vulgaris in Adult Patients With Combined Liquid Nitrogen Cryotherapy and Topically Applied Cantharidin


N/A
18 Years
65 Years
Not Enrolling
Both
Verruca Vulgaris

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Trial Information

A Randomized Clinical Trial Examining the Efficacy of Treatment of Cutaneous Verruca Vulgaris in Adult Patients With Combined Liquid Nitrogen Cryotherapy and Topically Applied Cantharidin


Inclusion Criteria:



1. common warts on non-genital, non-facial skin

2. otherwise healthy

3. between 18-65 and able to give informed consent

4. capable of tolerating treatment

Exclusion Criteria:

1. Ill-health

2. Poor tolerance or sensitivity to treatments in study

3. <18 years old; >65 years old

4. verruca plana or condyloma acuminata

5. immunosuppression or immune dysfunction

6. significant peripheral vascular disease

7. significant sensitivity to cold

8. epidermodysplasia verruciformis

9. mosaiform warts or periungual warts

Type of Study:

Interventional

Study Design:

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Outcome Measure:

Percentage of common warts cleared

Outcome Description:

Percentage of treated warts cleared with treatment, as measured with dermatoscopic examination, after 12 weeks.

Outcome Time Frame:

12 weeks

Safety Issue:

No

Principal Investigator

Richard A Flygare, PhD

Investigator Role:

Principal Investigator

Investigator Affiliation:

TUI University; North Idaho Dermatology

Authority:

United States: Institutional Review Board

Study ID:

NID-001

NCT ID:

NCT01084824

Start Date:

June 2007

Completion Date:

September 2008

Related Keywords:

  • Verruca Vulgaris
  • Warts
  • Verruca vulgaris
  • Liquid Nitrogen
  • Cantharidin
  • combination treatment
  • Warts

Name

Location
North Idaho Dermatology Coeur D'Alene, Idaho  83814