Cantharidin Application in Patients With Common Warts (Verruca Vulgaris) (COVE-3)
NCT07637734
Common Warts, Common Warts (Verruca Vulgaris)
Overland Park, Kansas, United States
View Trial DetailsNCT Number: NCT06973473
To assess the clinical efficacy and safety of topical imiquimod 5% cream combined with cryotherapy versus either of theme alone for the treatment of common warts by clinical and dermoscopic assessments.
Trial opening soon.
Get Notified18 year–60 year
All sexes
Observational
Topical Imiquimod 5% cream Combined with Cryotherapy Versus either of them alone in Treatment of Common Warts: A prospective Randomized Comparative Trial
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: 12 weeks
Assessment of complete warts clearance rate at 12weeks to evaluate the efficacy of combination therapy ( imiquimod5%cream+cryotherapy ) compared to topical imiquimod5%cream alone or cryotherapy alone in patients with common wart.
Contact information is provided by the study sponsor or research team.
Eman Fathy Ahmed Lecturer of Dermatology, Venereology and Andrology Faculty of
CONTACT
Assiut University
Other
Aprospective,Randomized,Comparative Clinical Trial of Combination Therapy of Imiquimod 5%Cream and Cryotherapy vs Monotherapy for Common Warts.
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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