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Treatment of common warts with topical solution of potassium hydroxide 15%

Comparison of efficacy and side effects of topical 15% potassium hydroxide solution and cryotherapy in the treatment of common wart.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014081118765N1
Enrollment
29
Registered
2014-12-12
Start date
2012-09-22
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Common wart. Verruca Vulgaris

Interventions

Intervention 1: Intervention group: Drug: Topical solution of 15% Potassium hydroxide Direct education to patients. Period of application: Disappearance of warts Application: Cotton swap weltering i
Treatment - Drugs
Intervention group: Drug: Topical solution of 15% Potassium hydroxide Direct education to patients. Period of application: Disappearance of warts Application: Cotton swap weltering in solution of
Control group :Treatment with cryotherapy Application: One cotton swap be drowned in to nitrogen liquid then put on each wart for ten seconds and repeat it twice.

Sponsors

Ahvaz Jundishapur University of Medical Sciences, Vice Chancellor
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: patient who have common wart with diameter less than 5 mm, on the hand or foot bilaterally. Exclusion criteria: pregnancy; lactation; treatment during one recent month; secondary skin infection

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Reduced size of Common warts. Timepoint: Before intervention. Every week from starting of intervention to disappearance of all warts. Two months after the end of intervention. Method of measurement: observation; Ruler.

Secondary

MeasureTime frame
Side effects. Timepoint: Before intervention. Every week from starting of intervention to disappearance of all warts. Two months after the end of intervention. Method of measurement: observation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSalah Shohani

Ahvaz Jundishapur University of Medical Sciences

shohani.s@ajums.acir+98 61 1222 2114

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026