Efficacy of Tazarotene in Treatment of Verruca Plana

Sponsor
Zagazig University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05314127
Collaborator
(none)
80
1
4
7.6
10.6

Study Details

Study Description

Brief Summary

Verruca plana is a common skin infection with worldwide distribution. Approximately 10% of general population is infected with flat warts and it represents up to 18 % of the patients seeking treatment for warts. Verruca plana is not merely an infectious disease but also affects the quality of patients' life. Verruca plana causes major cosmetic and social concerns. Lesions' persistence and recurrence cause frustrations and psychological distress which motivate patients to seek different treatment strategies. Verruca plana commonly affects the school aged children which augments its effect on the psychological and social development of children with stigmatization and bullying are great risks. The available treatment strategies neither ensured complete clearance of the disease nor were free of side effects. Frequently used physical removal methods are operator dependent and commonly lead to irritation, local inflammation, scars, dyspigmentation, and disfigurement. In this study we evaluate the efficacy and the safety of tazarotene gel 0.1% in the treatment of verruca plana compared to imiquimod or 5-fluorouracil

Condition or Disease Intervention/Treatment Phase
Phase 2

Detailed Description

Patients will be assigned randomly into one of 4 groups as 1:1:1:1 using randomization.com with the seed number 7607

  • Group (A): Patients will be treated with topical tazarotene gel 0.1%with a cotton tipped applicator on every lesion once daily at night.

  • Group (B): Patients will be treated with topical 5- fluorouracil 5% cream applied once daily at night.

  • Group (C): Patients will be treated with imiquimod cream 5% applied once daily at night.

  • Group (D): Patients will be treated with petroleum jelly once daily at night.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
80 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Investigator)
Primary Purpose:
Treatment
Official Title:
Efficacy of Tazarotene Versus Topical 5-Fluorouracil, and Imiquimod in The Treatment of Verruca Plana
Actual Study Start Date :
Apr 15, 2022
Anticipated Primary Completion Date :
Oct 1, 2022
Anticipated Study Completion Date :
Dec 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Tazarotene

20 patients of verruca plana receiving daily topical Tazarotene 0.1% gel at night

Drug: Tazarotene 0.1% Gel,Top
once daily topical application at night with a cotton tipped applicator on every lesion

Active Comparator: Imiquimod

20 patients with verruca plana will be treated with imiquimod cream 5% applied once daily at night

Drug: Imiquimod
Imiquimod cream 5% applied once daily at night with a cotton tipped applicator applied once daily.

Experimental: 5- fluorouracil

20 patients with verruca plana will be treated with topical 5- fluorouracil 5% cream applied once daily at night

Drug: Fluorouracil Cream
5- Fluorouracil Cream 5% is applied once daily at night with a cotton tipped applicator

Placebo Comparator: Petrolatum

20 patients with verruca plana will be treated with petroleum jelly once daily at night.

Drug: Petrolatum
applied once daily at night

Outcome Measures

Primary Outcome Measures

  1. The proportion of patients with complete clearance of flat warts (Physician Wart Assessment scale PWA = 0) at the end in the four arms of the clinical trial. [Till complete clearance of all lesions or a maximum of 12 weeks, whichever came first]

    Complete clearance is defined by complete disappearance of the warts and return to normal skin markings

  2. The incidence of adverse events measured by the percentage of participants developing them in the four arms of the study [Till complete clearance of all lesions or a maximum of 12 weeks, whichever came first]

Secondary Outcome Measures

  1. The mean percent of warts achieving PWA 0 (complete clearance) per-participant across the different arms of the clinical trial [Till complete clearance of all lesions or a maximum of 12 weeks, whichever came first]

  2. The median time for participants to achieve clearance of all warts in the different arms of the clinical trial. [Till complete clearance of all lesions or a maximum of 12 weeks, whichever came first]

  3. The proportion of patients achieving poor response (<50% of warts disappeared) or partial response (> 50%-99% of warts disappeared) [Till complete clearance of all lesions or a maximum of 12 weeks, whichever came first]

  4. The quality of life index measured by the difference in the wart specific Dermatology Life Quality Index at the end of the trial compared to the baseline [at the end of 6 months period follow up]

  5. The patients' adherence to treatment measured by the percentage of patients withdrawn from each arm of the trial [at the end of 12 weeks study period]

  6. The patients' adherence to treatment measured by the percentage of missed doses in each arm of the trials [at the end of 12 weeks study period]

Eligibility Criteria

Criteria

Ages Eligible for Study:
4 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • All participants must be willing to sign informed consent; for patients younger than 18 years old, parents or guardians will sign an informed consent

  • Age > 4 years.

  • Both sexes.

  • Patients with clinically and dermoscopically diagnosed plane warts.

  • Subject is willing and able to follow all study instructions and to attend all study visits

Exclusion Criteria:
  • • History of hypersensitivity to any of the drugs used.

  • Pregnancy and lactation.

  • Patients with epidermodysplasia verruciformis syndrome.

  • Patients with eczematous skin disorders.

  • Presence of any active infections e.g. herpes, tuberculosis.

  • History of topical anti wart treatment within 4 weeks of recruitment to the study, and a 12-week period for systemic anti-wart treatment, or immunotherapy, or HPV vaccine in the last 24 weeks.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Dermatology department, Zagazig University Hospitals, Faculty of Medicine, Zagazig University Zagazig Select Region Egypt 44511

Sponsors and Collaborators

  • Zagazig University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Hagar Nofal, Lecturer, Principal Investigator, Zagazig University
ClinicalTrials.gov Identifier:
NCT05314127
Other Study ID Numbers:
  • 9326/22-2-2022
First Posted:
Apr 6, 2022
Last Update Posted:
May 16, 2022
Last Verified:
May 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
Yes
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
Yes
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 16, 2022