Skin Dryness and Soothing Effects of Benzoyl Peroxide Versus Polymer-Based Benzoyl Peroxide Formulations in Acne Treatment

A Comparative Clinical Study to evaluate the Skin Dryness and Soothing Effects of Benzoyl Peroxide Versus Polymer-Based Benzoyl Peroxide Formulations in Acne Treatment - NIL

Status

Active, not recruiting

Phases

Phase 4

Study type

Observational

Source

CTRI

Registry ID

CTRI/2026/01/100932

Enrollment

Registered

2026-01-13

Start date

Unknown

Completion date

Unknown

Last updated

2026-02-02

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

Conditions

None listed

Interventions

Intervention1: Test product: Benzoyl Peroxide: Test Product: Benzoyl Peroxide Dose: Apply 5 % Benzoyl peroxide is 2-3 times a day. Route of Administration: Topical (Acne affected area) Control Inter

Eligibility

Inclusion criteria

Inclusion criteria: 1.Gender: Male and Female(50:50) aged Between 18-35. 2.Non-pregnant, non-lactating female 3.Subject with acne and normal to oily skin. 4.Subject willing to give written informed consent 5.Women of child bearing potential must have a negative urine pregnancy test. 6.Free of any systemic and dermatologic disorder, which in the opinion of the investigator, will interface with the study results or increase the risk of AE. 7.Are willing to avoid prolonged exposure of the treatment area to ultraviolet radiation (natural or artificial) for the duration of the study.

Exclusion criteria

Exclusion criteria: 1.Subjects who are pregnant, breast feeding, or planning to become pregnant during the study 2.Subjects having Moderate to severe pigmentation, sunburn, scar or any type of skin concern. 3.Volunteers with skin conditions such as eczema, psoriasis, etc 4.Have any evidence of systematic cancer, squamous cell carcinoma, basal cell carcinoma in the last 5 years, or any other confounding skin condition. 5.Have open sore or open lesions in the treatment area 6. Have any condition that, in the opinion of the investigator, would confound the safety and efficacy assessments of the product. 7.Have participated in any interventional clinical trial in the previous 30 days. 8.Have a known sensitivity to any of the constituents of the test product including sensitivities to any of the constituents. 9.Have used, are using, or are planning to use immunosuppressive or immunomodulatory medications (i.e., biologics), including corticosteroids. 10.Have a history of alcohol or illegal drug/ substance abuse or suspected alcohol or illegal drug/substance abuse in the past 2 years.

Design outcomes

Primary

Measure	Time frame
Change in Skin Hydration Change in TEWL Change in Sebum Smoothness Acne countTimepoint: T0, T30min, T4hr, T8hr, T24hrs, T14days	—

Secondary

Measure	Time frame
Not ApplicableTimepoint: Not Applicable	—

Countries

India

Contacts

Public ContactPuneet Mittal

CCFT Laboratories

puneetmittal@mgcts.org08937015757

Outcome results