HygienePhase 3NCT00793026
Dermacyd Breeze Pocket BR (Lactic Acid) - Acceptability
A Phase 3 study testing Dermacyd Breeze Pocket BR (Lactic Acid) in people with Hygiene, run by Sanofi at 1 site in Brazil.
Trial summary
The purpose of this study is to prove the safety of the gynaecological formulation in normal conditions of use. Read more about this study
- Who is it for?
- Ages 18 to 60 years, women onlyHealthy volunteers can take part
- Conditions the study is for
- Hygiene
- What is being tested?
- Dermacyd Breeze Pocket BR (Lactic Acid)
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 30 participants
- Where
- 1 siteBrazil
- Study dates
- Nov 2008to Nov 2008
- Phase
- Phase 3
- 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 18 to 60 years
- Women only
- Healthy volunteers accepted
- Adult
Who may be able to join
- Integral skin test in the region;
- To use products of the same category;
Who cannot join
- Lactation or gestation;
- Use of anti-inflammatory, anti-histaminic or immunosuppressant drugs;
- Cutaneous disease (local or spread) in the evaluation area;
- Pathology which may cause immunity depression, such as HIV, diabetes;
- Endocrine pathology
- Solar exposure 15 days before evaluation;
Show all 9Show fewer
- Treatment until four months before the selection.
- Allergic or atopic history to cosmetics products
- The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Safety Dermatological Evaluation: Genital Mucous Irritation - Test in Use - Dermacyd Breeze Pocket BR (Lactic Acid).
The purpose of this study is to prove the safety of the gynaecological formulation in normal conditions of use.
- Conditions
- Hygiene
- Being tested
- Dermacyd Breeze Pocket BR (Lactic Acid)
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Dermacyd Breeze Pocket BR (Lactic Acid)Drug
Dermacyd Breeze Pocket BR (Lactic Acid) during 21 consecutive days
| Study group | Role | What they receive |
|---|---|---|
| 1 | Experimental | Dermacyd Breeze Pocket BR (Lactic Acid) Receives: Drug: Dermacyd Breeze Pocket BR (Lactic Acid) |
What is being measured
The primary outcome is the main question the study is designed to answer.
Absence of irritation
Measured: Throughout the study
Good acceptability
Measured: Throughout the study
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted18 Nov 2008 (estimated)
- Study startNov 2008
- Primary completionNov 2008
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for HygieneStudies of the same condition, open and under way.
- More trials run by SanofiThe sponsor's other registered studies.
- 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 3
- Primary purpose
- Supportive care
- Allocation
- Non-randomised
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 30 participants (actual)
Sponsor and investigators
- Lead sponsor
- Sanofi
- Sponsor type
- Industry (pharma, biotech, devices)
- Investigators
- Jaderson Lima, Study director, Sanofi
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00793026
- Sponsor's protocol ID
- LACAC_L_04365
- Status last verified
- Dec 2008
- First submitted
- 17 Nov 2008
- Last updated
- 19 Dec 2008
- Results posted
- No
Study at a glance
From the registry record, last updated by the sponsor on 19 Dec 2008. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Safety Dermatological Evaluation: Genital Mucous Irritation - Test in Use - Dermacyd Breeze Pocket BR (Lactic Acid).
- ClinicalTrials.gov ID
- NCT00793026
- Acronym / sponsor ID
- LACAC_L_04365
- Conditions
- Hygiene
- Phase
- Phase 3
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 30 participants (actual)
- Lead sponsor
- SanofiIndustry (pharma, biotech, devices)
- Study start
- Nov 2008
- Primary completion
- Nov 2008 (actual)
- First posted
- 18 Nov 2008 (estimated)
- 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.
The purpose of this study is to prove the safety of the gynaecological formulation in normal conditions of use.
Study design
- Primary purpose
- Supportive care
- Allocation
- Non-randomised
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| 1 | Experimental | Drug: Dermacyd Breeze Pocket BR (Lactic Acid)Dermacyd Breeze Pocket BR (Lactic Acid) |
Who may qualify
- Ages
- 18 to 60 years
- Sex
- Female only
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (2 listed)
- Integral skin test in the region;
- To use products of the same category;
Key exclusion criteria (9 listed)
- Lactation or gestation;
- Use of anti-inflammatory, anti-histaminic or immunosuppressant drugs;
- Cutaneous disease (local or spread) in the evaluation area;
- Pathology which may cause immunity depression, such as HIV, diabetes;
- Endocrine pathology
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 |
|---|---|---|
| Dermacyd Breeze Pocket BR (Lactic Acid)Dermacyd Breeze Pocket BR (Lactic Acid) during 21 consecutive days | Drug | 1 |
Primary outcome
Absence of irritation
Time frame: Throughout the study
Good acceptability
Time frame: Throughout the study
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 19 Dec 2008.
- Related InfoLink provided by the sponsor.
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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.
Jaderson Lima study director
Sanofi
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 3 study testing Dermacyd Breeze Pocket BR (Lactic Acid) in people with Hygiene, run by Sanofi at 1 site in Brazil.
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 2 inclusion and 9 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 19 Dec 2008. 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 Brazil. 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.
What does this phase mean?
Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
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?
Absence of irritation (time frame: Throughout the study). The study lists 2 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 19 Dec 2008; AzTrials last refreshed its copy on 30 Oct 2026.