Warts Clinical Trial
Official title:
Pivotal Study to Assess the Clinical Efficacy and Safety of Microwave Treatment in Warts
This is a multi-center, open, randomized, parallel-group, controlled, blind-assessed trial of approximately 124 subjects that require treatment for up to 5 common or plantar warts. Subjects will be randomized to one of two treatment groups: Microwave Treatment (Swift® system) or Cryotherapy.
The primary objective of this study is to collect evidence of the effectiveness of the Swift device for the treatment of common and plantar warts and compare with Cryotherapy. The secondary objectives of this study are to collect evidence of the safety, effectiveness and patient experiences of the Swift device for the treatment of common and plantar warts and compare with Cryotherapy. Eligible subjects who provide written informed consent will be randomized to either Microwave Treatment or Cryotherapy. Each eligible subject will receive treatment at the baseline visit (Visit 2) and again 4-weeks later. Subjects will receive a minimum of 2 treatments or, if further treatment is required, up to a maximum of 4 treatments; each treatment is given in 4-week intervals. Follow-up is 12-weeks after the last treatment has been administered where the warts will be assessed for resolution. Further follow-up visits occur 6-months and 12-months after the last treatment where the warts will be assessed for resolution or reoccurrence (if resolved at the 12-week visit). ;
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT01757392 -
Candin Safety & Efficacy Study for the Treatment of Warts
|
Phase 2 | |
Completed |
NCT00973856 -
Evaluation of the Effectiveness of an Alcohol Based Hand Gel for the Reduction of Warts on the Hands
|
N/A | |
Completed |
NCT02902822 -
Tele-dermatology of Skin Cancer in a Cohort of Local Health Authority Employees in the Province of Bergamo
|
N/A | |
Withdrawn |
NCT00546611 -
The Purpose of This Study is to Determine Whether Topical Application of PEP005 is Safe for the Treatment of Common Wart(s)
|
Phase 1 | |
Completed |
NCT00117871 -
Study With a Topical Gel to Treat Common Warts in Adults
|
Phase 2 | |
Completed |
NCT04278573 -
Intralesional Vitamin D Injection for Treatment of Common Warts
|
Phase 2 | |
Completed |
NCT02231879 -
Plerixafor Versus G-CSF in the Treatment of People With WHIM Syndrome
|
Phase 2/Phase 3 | |
Completed |
NCT06309420 -
Clinical Trial to Evaluate Efficacy and Safety of a Cryogenic Medical Device for Treatment of Common and Plantar Warts
|
N/A | |
Not yet recruiting |
NCT05616078 -
Laser Versus Cryotherapy for the Treatment of Recalcitrant Warts
|
N/A | |
Not yet recruiting |
NCT05617950 -
Salicylic Acid Versus Cryotherapy for the Treatment of HPV1-induced Plantar Warts
|
N/A | |
Recruiting |
NCT01712295 -
17% Salicylate Versus 17% Salicylate-Ethyl Pyruvate for Plantar Foot Warts
|
Phase 4 | |
Active, not recruiting |
NCT00254280 -
Treatment of Recalcitrant Hand and Foot Warts With Intense Pulsed Light - a Randomized Controlled Trial
|
N/A | |
Completed |
NCT04781244 -
Cost-effectiveness of EndWarts® FREEZE - an Alternative Home Cryotherapy Device for Wart Treatment
|
N/A | |
Completed |
NCT01101750 -
Does the HPV Vaccine Cause the Same Response in Adolescent Kidney and Liver Transplant Patients as in Healthy Controls?
|
Phase 4 | |
Completed |
NCT03487549 -
Cantharidin and Occlusion in Verruca Epithelium
|
Phase 2 | |
Recruiting |
NCT05625633 -
Human Papillomavirus (HPV) Vaccination vs. Placebo for the Treatment of Refractory Cutaneous Warts
|
Phase 2/Phase 3 | |
Completed |
NCT02393417 -
Safety and Efficacy of Varying Regimens of CANDIN for Treatment of Common Warts (Verruca Vulgaris)
|
Phase 2 | |
Completed |
NCT01808443 -
Efficacy of Laser Versus Cryotherapy in the Treatment of Warts
|
N/A | |
Completed |
NCT00116662 -
An up to Twelve Week Safety and Efficacy Study With a Topical Gel to Treat Common Warts in Pediatric Subjects
|
Phase 2 | |
Completed |
NCT00116675 -
Four Week Safety and Efficacy Study With a Topical Gel to Treat Common Warts in Pediatric Subjects
|
Phase 2 |