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OpenTrials
Completed

NCT Number: NCT05503784

Study to Evaluate the Efficacy of Bite's Natural Deodorant

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.

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Key information

Conditions

Age range

24 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Citruslabs

Santa Monica, California, 90404, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

BITE Deodorant

Other

BITE natural Deodorant

Primary outcomes

  1. Changes in underarm odor

    Time frame: 4 weeks

    Survey-based assessment (0-5 scale) of changes in underarm odor

  2. Changes in clothing staining

    Time frame: 4 weeks

    survey-based assessment (0-5 scale) of changes in clothing staining

  3. Changes in reported quality of life

    Time frame: 4 weeks

    survey-based assessment (0-5 scale) of changes in reported quality of life

Sponsors and collaborators

Lead sponsor

Kind Lab PBC.

Industry

Collaborators

  • Citruslabs

Registry information

Important dates

Study start
2021
Primary completion
2022
Study completion
2022
First posted
Aug 17, 2022
Registry last updated
Aug 17, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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