Study to Evaluate the Efficacy of Bite's Natural Deodorant

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT05503784

Enrollment

Registered

2022-08-17

Start date

2021-11-26

Completion date

2022-03-11

Last updated

2022-08-17

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

Conditions

Sweat, Underarm Odor

Keywords

sweat, underarm odor, perspiration

Brief summary

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.

Interventions

OTHERBITE Deodorant

BITE natural Deodorant

Study design

Allocation

Intervention model

SINGLE_GROUP

Primary purpose

OTHER

Masking

NONE

Intervention model description

Open label

Eligibility

Sex/Gender

ALL

Age

24 Years to 65 Years

Healthy volunteers

Yes

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

Design outcomes

Primary

Measure	Time frame	Description
Changes in underarm odor	4 weeks	Survey-based assessment (0-5 scale) of changes in underarm odor
Changes in clothing staining	4 weeks	survey-based assessment (0-5 scale) of changes in clothing staining
Changes in reported quality of life	4 weeks	survey-based assessment (0-5 scale) of changes in reported quality of life

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026