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Clinical Study for Perceived Effectiveness Evaluation of Moisturizing Action of Intimate Use Product in Postmenopausal Women

Clinical Study for Perceived Effectiveness Evaluation of Moisturizing Action of Intimate Use Product in Postmenopausal Women

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02434887
Acronym
CLIN ST EF EV
Enrollment
26
Registered
2015-05-06
Start date
2015-06-30
Completion date
2015-08-31
Last updated
2015-11-10

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

Conditions

Female Dry Genital Mucosa

Brief summary

The purpose of this study is to verify the effectiveness of the investigational product through Subjective Assessment and answered by volunteers.

Interventions

Sponsors

Kley Hertz S/A
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
FEMALE
Age
45 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Female aged between 45 to 65 years old * Sexually active volunteers, with a minimum of 1 intercourse per week * In menopause for at least 6 months; * Intact skin in the product analysis region; * No prior reactions to topical products * Reading, understanding, agreement and signature of the informed consent form

Exclusion criteria

* Use of anti-inflammatory and immunosuppressive ( in the last 30 days and during the study) * Active skin diseases (local or disseminated) in the evaluation área; * Diseases that cause imune suppression; * Endocrine disorders such as thyroid, ovarian or adrenal gland disorders; * Any infection in the region where the product will be analyzed diagnosed at enrollment; * Other conditions considered by the investigator physician as reasonable for the disqualification of the individual's participation in the study.

Design outcomes

Primary

MeasureTime frame
Evaluation of the product's efficiency as a moisturizer through subjective evaluation40 days

Outcome results

None listed

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