ClinicalTrials.gg
Not yet recruitingNCT07927920Updated Nov 10, 2026

Salicylic Acid Solution Versus Tretinoin 0.05% Cream for Treating Plane Warts

An interventional study of Salicylic acid solution (15-17%) and Tretinoin 0.05% cream in Plane Warts, sponsored by Combined Military Hospital, Pakistan. Not yet recruiting at 1 site in Pakistan. Open to participants aged 12 Years to 40 Years. Per ClinicalTrials.gov, last updated 2026-11-10.

Sponsored by Combined Military Hospital, Pakistan · Not applicable, Interventional, and Treatment

Updated Nov 10, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
200
Allocation
Randomized
Ages
12 Years to 40 Years
Sex
All
01

Study summary

This randomized controlled trial aims to compare the effectiveness and safety of topical salicylic acid solution (15-17%) and tretinoin 0.05% cream in treating plane warts. A total of 200 patients aged 12-40 years will be recruited from the Dermatology Department of Combined Military Hospital (CMH), Abbottabad, and randomly divided into two treatment groups. Both treatments will be applied once daily at night for 12 weeks, with follow-up visits at weeks 4, 8, and 12. The primary outcome will be complete clearance of all warts at 12 weeks, while adverse effects such as redness, scaling, burning, itching, and pigmentation changes will also be assessed. The study aims to identify which treatment offers better efficacy and tolerability to support evidence-based treatment decisions for patients with plane warts.This randomized controlled trial aims to compare the effectiveness and safety of topical salicylic acid solution (15-17%) and tretinoin 0.05% cream in treating plane warts. A total of 200 patients aged 12-40 years will be recruited from the Dermatology Department of Combined Military Hospital (CMH), Abbottabad, and randomly divided into two treatment groups. Both treatments will be applied once daily at night for 12 weeks, with follow-up visits at weeks 4, 8, and 12. The primary outcome will be complete clearance of all warts at 12 weeks, while adverse effects such as redness, scaling, burning, itching, and pigmentation changes will also be assessed. The study aims to identify which treatment offers better efficacy and tolerability to support evidence-based treatment decisions for patients with plane warts

02

Conditions studied

  • Plane Warts

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03

In context

Warts

171 studies on the registry are indexed under Warts; 35 are open to participants now.

This study's planned enrollment of 200 is above the median of 70 across 155 interventional studies indexed under Warts.

Browse Warts studies →

Lead sponsor

Combined Military Hospital, Pakistan is the lead sponsor of 15 studies on the registry; 4 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
12 Years to 40 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Patients of both genders
  2. Age 12 to 40 years
  3. Clinically diagnosed plane warts (≥5 lesions)
  4. Warts present for at least 4 weeks
  5. Treatment-naive or no treatment in last 4 weeks

Exclusion criteria

Exclusion Criteria:

  1. Pregnancy or lactation (for females of childbearing age)
  2. Known to salicylic acid or tretinoin
  3. Active facial dermatitis or eczema
  4. patients
  5. Concurrent use of other wart treatments
  6. Facial scarring that would interfere with assessment
  7. Use of systemic retinoids in past 6 months
Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Hypersensitivity

An allergy, or another reaction of the immune system, to a substance. “Hypersensitivity to the study drug” means a known allergic reaction to it — not every side effect a medicine can have.

Immunosuppression

A weakened immune system. It can come from an illness, such as HIV or some blood cancers, or from medicines that turn the immune system down, for example after an organ transplant or for an autoimmune disease; steroids at higher doses count.

Read whether the line is about a condition or about medicines, and which medicines and doses it means.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
200 participants (estimated)

Study arms

  • Active comparator
    Group A

    Group A (salicylic acid): Salicylic acid 15-17% solution will be provided to the patients and advised to apply the solution only once daily, especially at night time to the infected areas and let it remain there for 6-8 hours. Afterwards, it should be washed in the morning time.

    Drug: Salicylic acid solution (15-17%)

  • Active comparator
    Group B

    Group B (tretinoin): Tretinoin 0.05% cream will be prescribed to the patients. They will be advised to apply the cream only once daily, especially at night time to the infected areas.

    Drug: Tretinoin 0.05% cream

Interventions

  • DrugSalicylic acid solution (15-17%)

    Group A (salicylic acid): Salicylic acid 15-17% solution

  • Group B (tretinoin): Tretinoin 0.05% cream

06

What researchers measure

Primary outcomes

  1. Proportion of patients achieving complete clearance of plane wart lesions at 12 weeks, defined as 100% clearance of all wart lesions, compared between the salicylic acid solution and tretinoin 0.05% cream treatment groups.

    Time frame: 12 weeks

Secondary outcomes

  1. Change in Wart Lesion Count at 12 Weeks

    Percentage reduction in the number of plane wart lesions from baseline to 12 weeks, categorized as: * Complete clearance: 100% reduction * Marked improvement: 75-99% reduction * Moderate improvement: 50-74% reduction * Mild improvement: 25-49% reduction * No response:

    Time frame: 12 weeks

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for Dec 2026; primary completion for May 2027, 5 months later.

Of 28 interventional studies with no phase under Warts, half reached primary completion within 10 months of starting (the median), counting those still running; a quarter within 6 and three quarters within 31. This study's planned 5 months is below that.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 25, 2026
First posted
Nov 10, 2026
StartEst.
Dec 2026
Primary completionEst.
May 2027
CompletionEst.
Jul 2027
Last update
Nov 10, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Nov 10, 2026
Show all 1 update
  1. Nov 10, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07927920
Lead sponsor
Combined Military Hospital, Pakistan
Responsible party
Aqsa Gul (Resident Dermatology, Combined Military Hospital Abbottabad) — Principal investigator
First posted
Nov 10, 2026
Start date
Dec 2026 (estimated)
Primary completion
May 2027 (estimated)
Completion
Jul 2027 (estimated)
Last update
Nov 10, 2026

Study contacts

Aqsa Gul
Contact
gulaqsa920@gmail.com
+923326903184

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Nov 2026. You cannot join it, but the record below documents what was studied.

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Discussion

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Studies of the drug tested here: Tretinoin

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