Anti-pigmentation and Anti- Perspirant activity of Bright and Breezy Forest Dew Underarm Roll On

A Clinical Study to Evaluate Anti-pigmentation and Anti- Perspirant activity of Bright and Breezy Forest Dew Underarm Roll On - NIL

Status

Active, not recruiting

Phases

Phase 4

Study type

Observational

Source

CTRI

Registry ID

CTRI/2026/07/113234

Enrollment

Registered

2026-07-02

Start date

Unknown

Completion date

Unknown

Last updated

2026-08-03

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- Bright and Breezy Forest Dew Underarm Roll On: Test Product- Bright and Breezy Forest Dew Underarm Roll On Route of Administration: Topical Frequency: 2 times a day for 14

Eligibility

Inclusion criteria

Inclusion criteria: 1. Subjects between 18 and 45 years. 2. Subject with pigmented underarm. 3. Volunteer with Excess Sweat and Smell in underarm. 4. Having apparently healthy skin on test area. 5 For whom the investigator considers that the compliance will be correct. 6. Cooperating, informed of the need and duration of the examinations and ready to comply with protocol procedures. 7. Having signed a Consent Form. 8. Willingness to avoid excessive water contact for example swimming 9.Should be able to read and write in English, Hindi or local language. 10. Having valid proof of identity and age.

Exclusion criteria

Exclusion criteria: 1. Dermatological infection or pathology on the level of studied area. 2. Hypersensitivity, allergy antecedent to any cosmetic product, raw material. 3. Any clinically significant systemic or cutaneous disease, which may interfere with study treatment or procedures. 4. Chronic illness which may influence the outcome of the study Subjects on any medical treatment either systemic or topical which may interfere with the performance of the study treatment presently or in the past 1 month. 5. Subject in an exclusion period or participating in another food, cosmetic or therapeutic trial.

Design outcomes

Primary

Measure	Time frame
1. Change in Odour Intensity Timepoint: At T0 min, T+30 min, T+4 hours, T+8 hours, T+24 hours and T+48 hours	—

Secondary

Measure	Time frame
1. Change in pigmentation 2. HD ImagingTimepoint: At Day 0 and Day 14;1.Dermat EvaluationTimepoint: At Day 0, 30 min and Day 14;SGATimepoint: At Day 14	—

Countries

India

Contacts

Public ContactPuneet Mittal

CCFT Laboratories

puneetmittal@mgcts.org08937015757

Outcome results