Long Lasting Freshness of Bohem Antiperspirant Roll-On

A Clinical Study to Evaluate Long Lasting Freshness of Bohem Antiperspirant Roll-On on healthy human subjects - NIL

Status

Active, not recruiting

Phases

Phase 4

Study type

Observational

Source

CTRI

Registry ID

CTRI/2024/11/077264

Enrollment

Registered

2024-11-25

Start date

Unknown

Completion date

Unknown

Last updated

2025-09-15

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- Bohem Antiperspirant Roll-On: Test Product- Bohem Antiperspirant Roll-On, Route of Administration: Topical Frequency: Once Duration:48hrs Control Intervention1: Not Appli

Eligibility

Inclusion criteria

Inclusion criteria: 1. Voluntary man or women between 18 and 50 years. 2. Known issue of body odour. 3. Having apparently healthy skin on test area. 4. For whom the investigator considers that the compliance will be correct. 5. Cooperating, informed of the need and duration of the examinations and ready to comply with protocol procedures. 6. Having signed a Consent Form. 7. Volunteer with Excess Sweat and Smell in Arm Pit. 8. Willingness to avoid excessive water contact (for example swimming) or activity which causes excessive sweating (that is exercise, sauna), during the course of the study. 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. Pregnant or nursing mothers 2.Dermatological infection or pathology on the level of studied area 3.Hypersensitivity, allergy antecedent (to any cosmetic product, raw material ) 4.Any clinically significant systemic or cutaneous disease, which may interfere with study treatment or procedures. 5.Chronic illness which may influence the outcome of the study 6.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) 7.Subject in an exclusion period or participating in another food, cosmetic or therapeutic trial.

Design outcomes

Primary

Measure	Time frame
- Fragrance intensity change - Odour intensity change by Odourmeter. - Local Irritation assessment (Safety)Timepoint: At T0, T24hrs, T48hrs	—

Secondary

Measure	Time frame
Not ApplicableTimepoint: Not Applicable	—

Countries

India

Contacts

Public ContactPuneet Mittal

CCFT Laboratories

puneetmittal@mgcts.org8937015757

Outcome results