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Plantar Warts clinical trials

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NCT ID: NCT02861404 Terminated - Plantar Warts Clinical Trials

Evaluation of Viral Status of Patients With Plantar Warts Included in VRAIE Study, Non-responder to Study Treatment

BIOVRAIE
Start date: April 2010
Phase: N/A
Study type: Observational

The principal objective of the study is the evaluation of the role of Human Papilloma Virus (HPV) in plantar warts (prevalence, genotype), resistant or not, treated or not, cured or not. This epidemiological study is an ancillary study of the prospective, randomized controlled, clinical study VRAIE (sponsor: APHP) comparing 5 usual strategies in the management of plantar warts.

NCT ID: NCT02640820 Active, not recruiting - Common Warts Clinical Trials

Evaluate the Effectiveness and Safety of DPCP Ointment (Samcyprone™) on the Clearance of Verruca Vulgaris (Common Warts)

Start date: December 2015
Phase: Phase 2
Study type: Interventional

Warts are benign epidermal tumors caused by human papillomaviruses (HPVs). The active pharmaceutical ingredient DPCP has been used for many years as a compounded formulation in acetone for the treatment of warts, alopecia areata and more recently, cutaneous metastatic melanoma lesions. An improved topical ointment formulation of DPCP called Samcyprone™ will be evaluated for the treatment of common warts.

NCT ID: NCT02338336 Completed - Plantar Warts Clinical Trials

A Phase I/II Double-blind Study to Evaluate the Safety and Efficacy of Nowarta110 in Patients With Plantar Warts Successfully Completed

Start date: February 2015
Phase: Phase 1/Phase 2
Study type: Interventional

To evaluate drug safety and efficacy in patients treated with Nowarta110 and to determine therapeutic activity against Plantar Warts - Clinical Tolerance - Clinical Recovery - Evaluate Safety

NCT ID: NCT01330615 Recruiting - Plantar Warts Clinical Trials

Efficacy Trial of Eutectic Lidocaine/Prilocaine Cream 5% (EMLA) for Analgesia Prior to Cryotherapy of Verrucae Plantaris

Start date: February 2010
Phase: N/A
Study type: Interventional

Aims: The investigators main purpose is to assess the efficacy of analgesia provide by topical lidocaine/prilocaine cream 5% (EMLA)® to pared plantar warts prior to application of liquid nitrogen cryotherapy in adults.

NCT ID: NCT01059110 Terminated - Plantar Warts Clinical Trials

Comparison of Five Treatments in Patients With Plantar Warts

VRAIE
Start date: February 2010
Phase: Phase 4
Study type: Interventional

The principal objective of the study is to compare 5 usual strategies in the management of plantar warts which did not cure after 5 weeks of a salicylate ointment given just prior the trial. The trial will include immunocompetent patients coming from the community and should help the office-based dermatologists and hospital in the decision-making therapeutic process.