Comparison of Efficacy of Topical Adaplene Gel Versus Crythotherapy in Recurrent Plantar Warts
1 other identifier
interventional
98
1 country
1
Brief Summary
This is a comparative study between two treatment options for skin viral infection.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for phase_4
Started Sep 2025
Shorter than P25 for phase_4
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
May 21, 2025
CompletedFirst Posted
Study publicly available on registry
June 11, 2025
CompletedStudy Start
First participant enrolled
September 15, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 15, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
September 15, 2026
ExpectedApril 29, 2026
April 1, 2026
5 months
May 21, 2025
April 23, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Efficacy of Treatment
It will be defined through visual inspection by observing the complete clearance of the warts after 8 weeks administration of the treatment in both groups
06 months
Study Arms (2)
A
EXPERIMENTALTreated with Topical adapalene gel 0.1%
B
EXPERIMENTALTreated with liquid nitrogen over affected parts
Interventions
Topical adapalene is a retinoid that helps in epidermal changes. Cryotherapy is a liquid nitrogen applied to affected parts for 6 months
Eligibility Criteria
You may qualify if:
- Patients age limit 18-60 Years Patients with either gender (Male/Female) Patients with recurrent plantar warts
You may not qualify if:
- Pregnancy/lactation. Pt on topical or systemic therapy in last 6 months. On immunosuppressants. \> 5 lesions. Pts with local secondary infections.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Khyber Teaching Hospital
Peshawar, Khyber Pakhtunkhwa, 25000, Pakistan
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Saba Naz, MBBS
Khyber Teaching Hospital
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- phase 4
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- DOCTOR
Study Record Dates
First Submitted
May 21, 2025
First Posted
June 11, 2025
Study Start
September 15, 2025
Primary Completion
February 15, 2026
Study Completion (Estimated)
September 15, 2026
Last Updated
April 29, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will not share
Patient's confidentiality may be breached