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Warts clinical trials

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NCT ID: NCT03210337 Completed - Common Wart Clinical Trials

A Phase2 of A-101 Topical Solution in Subjects With Common Warts

Start date: August 1, 2017
Phase: Phase 2
Study type: Interventional

The primary objective of this study is to evaluate the effectiveness of A-101 compared to vehicle when applied to 1 common target wart on the trunk or extremities.

NCT ID: NCT03183765 Completed - Plantar Wart Clinical Trials

Intralesional Measles, Mumps, Rubella (MMR) Vaccine Versus Cryotherapy in Treatment of Multiple Common and Planter Warts

Start date: August 1, 2017
Phase: Phase 4
Study type: Interventional

Warts are benign epidermal tumors caused by human papilloma virus, which are epitheliotropic non-enveloped double stranded DNA viruses. Transmission of warts occurs from direct person-to-person contact or indirectly by fomites . Warts appear in various forms including verruca vulgaris, plane, plantar, filiform, digitate and periungual.

NCT ID: NCT03129373 Completed - Warts Clinical Trials

Clinical Study : Efficacy and Safety of Three Cryotherapy Devices for Wart Treatment

Start date: July 2015
Phase: N/A
Study type: Interventional

The present study was set-up to evaluate clinical efficacy of Pixie® cryogenic pen versus two comparator cryogenic products (Wartner® and Wortie®) for the treatment of common and plantar warts.

NCT ID: NCT02971891 Completed - Clinical trials for Cutaneous Common Warts

A Phase 3 Study to Evaluate the Efficacy and Safety of CLS006 Versus Vehicle in Subjects 2 Years of Age or Older With Cutaneous Common Warts

Start date: January 2017
Phase: Phase 3
Study type: Interventional

To evaluate the efficacy and safety of six (6) weeks of once daily application of Furosemide Topical Gel 0.125% (CLS006) compared to vehicle in subjects ≥ 2 years of age with nongenital cutaneous common warts (verruca vulgaris).

NCT ID: NCT02902822 Completed - Melanoma Clinical Trials

Tele-dermatology of Skin Cancer in a Cohort of Local Health Authority Employees in the Province of Bergamo

Start date: October 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to demonstrate the validity and utility of a tele-dermatology system in the midterm periodic screening of non-widespread skin lesions of recent onset or for which a specialized early classification is deemed to change the prognosis - including precancerous skin lesions as well as melanoma and non-melanoma skin cancers - compared to control visits at fixed follow-up.

NCT ID: NCT02798419 Completed - Common Warts Clinical Trials

Active-Controlled Study to Assess the Efficacy and Safety of DFD-05 in Subjects With Common Warts

Start date: January 2016
Phase: Phase 2
Study type: Interventional

DFD05 vs. Active01 in the treatment of common warts

NCT ID: NCT02773719 Completed - Wart Clinical Trials

Biofields Therapy on Warts

MAGNETIK
Start date: April 2016
Phase: N/A
Study type: Interventional

Traditionally, healers are willing to look after, two out of three French citizens have already appealed to them at least once during their lives. Many healers in good faith are exercising their magnetism as a "gift" often inherited from elders. Now, they create interest of doctors who do not hesitate in some cases to ensure their cooperation, to implicitly recognize their mysterious talents. Some serious studies have examined these practices: Several studies have been conducted on the influence of biofield therapies in pain, depression and fatigue in cancer disease. The investigators propose a study of the effect of magnetism on the wart disease whose cure is objectively assessable. Sixty-two subjects in total would be included, comparing 2 proportions observed: the proportion of healing in the group treated with a "real" biofield therapist (recognized and affiliated to the National Group for Alternative Medicine in France) to the proportion of healing in the group treated with a "fake" biofield therapist (someone assessed as not having capacity to magnetize). The "fake" biofield therapist, placebo, has been trained to replicate gestures during a training validated by an independent recognized biofield therapist.

NCT ID: NCT02748902 Completed - Verruca Vulgaris Clinical Trials

Exploratory Study of Efficacy and Safety of Ingenol Mebutate 0.05% Gel for Common Warts on the Hands.

Start date: April 27, 2016
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine if ingenol mebutate 0.05% gel is safe and effective in treating common warts on the hands.

NCT ID: NCT02669862 Completed - Common Warts Clinical Trials

A Study of A-101 Solution in Subjects With Common Warts.

Start date: December 21, 2015
Phase: Phase 2
Study type: Interventional

This is a randomized, double-blind, vehicle-controlled, parallel-group study with 3 treatment groups.

NCT ID: NCT02650466 Completed - Common Warts Clinical Trials

Nanopulse Efficacy Study for the Treatment of Common Warts

Start date: December 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if the Nanopulse System can be used to clear common wart lesions on the skin. The Nanopulse System uses a series of low energy, high voltage pulses, each one several billionths of a second in duration, to effectively kill the target tissue contained within the applicator tip electrodes with minimal damage to surrounding tissue. Efficacy and patient outcomes are expected to equal or surpass current treatment modalities in terms of increased ease of use, faster patient healing and minimal scarring with fewer complications resulting from treatment. The device emits significantly less energy than existing electro-surgery or electro-cautery equipment and is believed to be similar to laser therapy treatment of warts. Trained clinicians can usually diagnose warts based by their appearance and location . Non-genital warts are subcategorized into common, periungual, flat, filiform, and plantar types. Common warts are benign, often skin-colored, or brown-grey, rough, bumpy growths on the hands and feet (caused by Human Papilloma Virus type 2) . Common warts in individuals without any immune deficiencies are low risk and are the focus of this study.Based upon the preclinical profile of the Nanopulse device, particularly its safety profile and its effect on transformed cells, it is hypothesized that application of pulses from the Nanopulse System , will result in complete clinical clearance of Common Wart lesions with minimal scarring.