SweatNCT05503784
Study to Evaluate the Efficacy of Bite's Natural Deodorant
A study testing BITE Deodorant in people with Sweat and Underarm Odor, run by Kind Lab PBC. at 1 site in United States.
Trial 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… Read more about this study
- Who is it for?
- Ages 24 to 65 yearsHealthy volunteers can take part
- Conditions the study is for
- Sweat, Underarm Odor
- What is being tested?
- BITE Deodorant
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 38 participants
- Where
- 1 siteUnited States
- Study dates
- 26 Nov 2021to 11 Mar 2022
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 24 to 65 years
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- 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
Who cannot join
- 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
Trial locations and contacts
1 site in 1 country.
About this study
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.
- Conditions
- Sweat, Underarm Odor
- Being tested
- BITE Deodorant
- Keywords
- sweat, underarm odor, perspiration
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
BITE DeodorantOther
BITE natural Deodorant
| Study group | Role | What they receive |
|---|---|---|
| Bite Deodorant | Experimental | All 38 participants apply BITE deodorant daily for four weeks. Receives: Other: BITE Deodorant |
What is being measured
The primary outcome is the main question the study is designed to answer.
Changes in underarm odor
Survey-based assessment (0-5 scale) of changes in underarm odor
Measured: 4 weeks
Changes in clothing staining
survey-based assessment (0-5 scale) of changes in clothing staining
Measured: 4 weeks
Changes in reported quality of life
survey-based assessment (0-5 scale) of changes in reported quality of life
Measured: 4 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted17 Aug 2022
- Study start26 Nov 2021
- Primary completion11 Mar 2022
- Study completion11 Mar 2022
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for SweatStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Other
- Allocation
- Not applicable
- Intervention model
- Single group
- Model description
- Open label
- Masking
- None (open label)
- Enrolment
- 38 participants (actual)
Sponsor and investigators
- Lead sponsor
- Kind Lab PBC.
- Sponsor type
- Industry (pharma, biotech, devices)
- Collaborators
- Citruslabs
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05503784
- Sponsor's protocol ID
- 20227
- Status last verified
- Aug 2022
- First submitted
- 15 Aug 2022
- Last updated
- 17 Aug 2022
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 17 Aug 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Study to Evaluate the Efficacy of Bite's Natural Deodorant
- ClinicalTrials.gov ID
- NCT05503784
- Acronym / sponsor ID
- 20227
- Conditions
- Sweat, Underarm Odor
- Keywords
- sweat, underarm odor, perspiration
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 38 participants (actual)
- Lead sponsor
- Kind Lab PBC.Industry (pharma, biotech, devices)
- Collaborators
- Citruslabs
- Study start
- 26 Nov 2021 (actual)
- Primary completion
- 11 Mar 2022 (actual)
- Study completion
- 11 Mar 2022 (actual)
- First posted
- 17 Aug 2022 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Study design
- Primary purpose
- Other
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
- Model description
- Open label
| Arm | Type | Receives |
|---|---|---|
| Bite Deodorant | Experimental | Other: BITE DeodorantAll 38 participants apply BITE deodorant daily for four weeks. |
Who may qualify
- Ages
- 24 to 65 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (7 listed)
- 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
Key exclusion criteria (8 listed)
- 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
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| BITE DeodorantBITE natural Deodorant | Other | Bite Deodorant |
Primary outcome
Changes in underarm odor
Time frame: 4 weeks
Survey-based assessment (0-5 scale) of changes in underarm odor
Changes in clothing staining
Time frame: 4 weeks
survey-based assessment (0-5 scale) of changes in clothing staining
Changes in reported quality of life
Time frame: 4 weeks
survey-based assessment (0-5 scale) of changes in reported quality of life
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 17 Aug 2022.
- Individual participant dataSharing planned: Undecided
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing BITE Deodorant in people with Sweat and Underarm Odor, run by Kind Lab PBC. at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 7 inclusion and 8 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 17 Aug 2022. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Changes in underarm odor (time frame: 4 weeks). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 17 Aug 2022.