Study to Evaluate the Efficacy of Bite's Natural Deodorant

Not Applicable

Completed

• Conditions: Sweat; Underarm Odor

• Registration Number: NCT05503784
• Lead Sponsor: Kind Lab PBC.

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.

Detailed Description

Not available

Study Timeline

• Study Start: 2021-11-26
• Primary Completion: 2022-03-11
• Study Completion: 2022-03-11
• Status Verified: 2022-08
• Study First Submitted: 2022-08-15
• Study First Submitted QC: 2022-08-15
• Last Update Submitted: 2022-08-15
• Study First Posted: 2022-08-17
• Last Update Posted: 2022-08-17

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 38

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

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Primary Outcome Measures

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

Trial Locations

Locations (1)

Citruslabs; 🇺🇸 Santa Monica, California, United States