Comparison of Cryotherapy and Peeling Agent in the Treatment of Common Warts

Sponsor
Combined Military Hospital Abbottabad (Other)
Overall Status
Completed
CT.gov ID
NCT05712811
Collaborator
(none)
60
1
2
6
10

Study Details

Study Description

Brief Summary

Objective: To compare the efficacy of cryotherapy using liquid nitrogen (cryoget method) versus trichloroacetic acid 90% (applicator method) in treatment of common warts.

Study Design: Randomized Control Trial. Place And Duration of Study: Department of Dermatology, CMH Abbottabad from Jun 2022 to Nov, 2022.

Condition or Disease Intervention/Treatment Phase
N/A

Detailed Description

A total of 60 patients were enrolled in this investigation by non-probability consecutive sampling technique. Sample size was calculated using WHO sample size calculator and patients were randomized into two equal groups, A and B, each comprising of 30 patients through lottery method. Patients with common warts such as hard lesions, raised lumps with rough surfaces at the back of their fingers, around nails and palm of their hands between the ages of 18 and 60 were included, whereas those with genital warts, cardiac, hepatic, renal, or hypercholesterolemia were excluded.

Study Design

Study Type:
Interventional
Actual Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Cryotherapy Versus Topical Tricholoacetic Acid 90% in Treatment of Common Warts
Actual Study Start Date :
Jun 1, 2022
Actual Primary Completion Date :
Nov 30, 2022
Actual Study Completion Date :
Nov 30, 2022

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Group A cryotherapy

Cryotherapy Group A had their warts treated once every two weeks for a total of twelve weeks, with liquid nitrogen using cryoget method for 10 to 15 seconds on each lesion (depending on size, until a narrow white rim of around 1 mm developed around it).

Drug: CRYOTHERAPY
Group A had their warts treated once every two weeks for a total of twelve weeks, with liquid nitrogen using cryoget method for 10 to 15 seconds on each lesion (depending on size, until a narrow white rim of around 1 mm developed around it).
Other Names:
  • Liquid nitrogen
  • Active Comparator: Group B Topical TCA 90%

    Topical TCA 90 % Warts in Group B were treated with liquid TCA 90% by an applicator every two weeks for a total of twelve weeks. After 20 minutes, patients were instructed to remove the solution by washing their warts with water or regular saline

    Drug: Tricholoracetic acid
    Group B were treated with liquid TCA 90% by an applicator every two weeks for a total of twelve weeks. After 20 minutes, patients were instructed to remove the solution by washing their warts with water or regular saline.
    Other Names:
  • Peeling agent
  • Outcome Measures

    Primary Outcome Measures

    1. Comparison of cryotherapy and Tricholoracetic acid 90% in treatment of common warts [12 weeks]

      Outcome was determined at the end of third month and the patients were labelled as cured and the efficacy was labelled as "Yes" in cases with absence of all the lesions. After twelve weeks of therapy, individuals with persistent warts were regarded as cases of treatment failure and efficacy was labelled as "No".

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 60 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Patient presented with common warts in dermatology opd
    Exclusion Criteria:
    • • Patients with warts on toes and tip of fingers

    • genital warts

    • cardiac, hepatic and renal disease

    • hypercholesterolemia

    • hypersensitivity reactions

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Cmh abbottabad Abbottābād Kpk Pakistan 22010

    Sponsors and Collaborators

    • Combined Military Hospital Abbottabad

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Dr kiran gul, Principal investigator, Combined Military Hospital Abbottabad
    ClinicalTrials.gov Identifier:
    NCT05712811
    Other Study ID Numbers:
    • CMHAbbottabad
    First Posted:
    Feb 6, 2023
    Last Update Posted:
    Feb 6, 2023
    Last Verified:
    Jan 1, 2023
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Feb 6, 2023