MC RCT - BPO vs Adapalene

Sponsor
University of Oklahoma (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05536882
Collaborator
(none)
150
1
2
18
8.3

Study Details

Study Description

Brief Summary

Non-blinded randomized controlled trial comparing efficacy of topical benzoyl peroxide 10% (vehicle choice per patient preference: e.g. gel, cream, lotion, wash) to topical adapalene 0.1% gel in the treatment of molluscum contagiosum in children aged 1 year old to 14 years old.

  • Two treatment wings: topical benzoyl peroxide 10% (vehicle choice per patient preference) applied 1-2x daily as tolerated vs adapalene 0.1% gel applied 1-2x daily as tolerated.

  • Primary outcome: Complete clearance at 12wks (defined as lack of identifiable papular molluscum contagiosum lesions on physical exam)

  • Secondary outcomes: % change in lesion count at 12wks.

Condition or Disease Intervention/Treatment Phase
  • Drug: Benzoyl peroxide
  • Drug: Adapalene Gel
Phase 3

Detailed Description

  • During the course of their normal workday, OU dermatology faculty and residents will be responsible for identifying and recruiting treatment-naïve patients being seen at the OU dermatology clinic for the diagnosis of molluscum contagiosum. These same faculty and residents will be responsible for approaching these patients regarding participation in the study. Chart review will not be a part of this selection process aside from what would naturally be done in the course of the patients' care. The same faculty and residents would be responsible for explaining the risks and benefits of study participation, obtaining written consent for study participation from a parent or guardian, obtaining verbal assent from patients aged 7-14 years old (as well as written assent for those capable of reading/writing), and randomizing patients to respective treatment wings using an online random number generator.

  • of MC lesions counted at time of recruitment, re-assessed at single follow up

appointment at 12wks

  • List of enrolled patients kept in excel spreadsheet on encrypted department shared drive. Data points added alongside patient names until all data points collected for an individual patient, then identifying information removed and replaced with a study number which will be used to refer to their de-identified data set going forward.

  • Patients/caregivers would be responsible for obtainment and application of respective medications (both medications available over the counter for < $15)

  • Primary and secondary outcomes will be assessed via Chi-square test

Study Design

Study Type:
Interventional
Anticipated Enrollment :
150 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Randomized Controlled Trial Comparing the Efficacy of Adapalene 0.1% Gel to 10% Benzoyl Peroxide in Treating Molluscum Contagiosum.
Anticipated Study Start Date :
Feb 1, 2023
Anticipated Primary Completion Date :
Aug 1, 2024
Anticipated Study Completion Date :
Aug 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Benzoyl peroxide

topical benzoyl peroxide 10% (vehicle choice per patient preference) applied 1-2x daily as tolerated until complete clearance or 12 week follow up

Drug: Benzoyl peroxide
See arm description

Active Comparator: Adapalene

adapalene 0.1% gel applied 1-2x daily as tolerated until complete clearance or 12 week follow up

Drug: Adapalene Gel
See arm description

Outcome Measures

Primary Outcome Measures

  1. Complete clearance at 12 weeks [12 weeks]

    Defined as lack of identifiable papular molluscum contagiosum lesions on physical exam at 12 week follow up visit

Secondary Outcome Measures

  1. % change in lesion count at 12 weeks [12 weeks]

Other Outcome Measures

  1. Incidence and severity of irritant contact dermatitis and other adverse events [12 weeks]

Eligibility Criteria

Criteria

Ages Eligible for Study:
1 Year to 14 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Children aged 1 year to 14 years old seen in an OU Dermatology resident or faculty clinic and diagnosed with molluscum contagiosum who have not received prior treatment for this condition, and whose parent/guardian(s) desire treatment for this condition.
Exclusion Criteria:
  • Patients who have received prior treatment for molluscum contagiosum.

  • Patients with a history of adverse reaction to any topical retinoid, benzoyl peroxide, cinnamon, or other benzoic derivatives (e.g., salicylic acid, hydroquinone, catechol, vanillin).

  • Pregnant females.

  • Patients with caregivers who do not speak English.

  • Patients with caregivers who are unable to provide consent.

  • Patients who decline to assent for participation.

Contacts and Locations

Locations

Site City State Country Postal Code
1 OU Health Department of Dermatology Oklahoma City Oklahoma United States 73104

Sponsors and Collaborators

  • University of Oklahoma

Investigators

  • Principal Investigator: Jason Hirshburg, MD, University of Oklahoma

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
University of Oklahoma
ClinicalTrials.gov Identifier:
NCT05536882
Other Study ID Numbers:
  • IRB# 14663
First Posted:
Sep 13, 2022
Last Update Posted:
Sep 13, 2022
Last Verified:
Sep 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
Yes
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University of Oklahoma
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 13, 2022