Study to Evaluate the Efficacy of Bite's Natural Deodorant

Kind Lab

Status

Completed

Conditions

Underarm Odor

Sweat

Treatments

Other: BITE Deodorant

Study type

Interventional

Funder types

Industry

Identifiers

NCT05503784

20227

Details and patient eligibility

About

This is an open-label observational single-arm clinical trial to study the efficacy of a commercial deodorant and its effect on odor, clothing (stains), and quality of life. It is hypothesized that the deodorant marketed as Bite deodorant will mask bodily odor in participants, will not stain clothes, and improve the quality of life in trial participants.

Enrollment

38 patients

Sex

All

Ages

24 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Agree to refrain from the use of any other deodorant or antiperspirant other than Bite for the study period
Must be in good health (does not report any medical conditions asked in the screening questionnaire)
Must be willing to comply with the requirements of the protocol
Must be willing to add the deodorant to their daily routine
Is willing and able to share feedback
Shower daily, and put deodorant on the first thing in the morning (before sweating)
If used deodorants previously must be a natural version

Exclusion criteria

Unwilling to follow the routine of the protocol
Currently participating in another research study
Severe chronic conditions including oncological conditions, psychiatric disease, or other
Females that are pregnant, want to become pregnant for the duration of the study, or who are breastfeeding
Presence of self-reported armpit sensitivity
Known to have severe allergic reactions
Have known allergies to the trial product ingredients
Currently using an antiperspirant