Status:
COMPLETED
A Clinical Investigation Into the Effectiveness and Safety of Five Water Based Personal Lubricants.
Lead Sponsor:
Reckitt Benckiser Healthcare (UK) Limited
Collaborating Sponsors:
proDERM GmbH
Conditions:
Dyspareunia
Vaginal Dryness
Eligibility:
FEMALE
18-65 years
Phase:
PHASE3
Brief Summary
This clinical investigation will look at the safety of five water based personal lubricants, and teir effectiveness the relief of intimate discomfort associated with vaginal dryness.
Detailed Description
This is an open label, five-arm, parallel-design clinical investigation determining the effectiveness and safety of five personal lubricants. This clinical investigation consists of two phases, a Tole...
Eligibility Criteria
Inclusion
- Subject has provided written informed consent.
- Subject is female and aged: 18 years to 65 years.
- Female subject in a mutually monogamous heterosexual relationship (≥ 3 months) who is sexually active, defined as having sexual intercourse at least once a week.
- Female subject of childbearing potential who is willing to use a highly effective method of contraception throughout the clinical investigation.
- Female subject that agrees to have a gynaecological pelvic examination to ensure no significant disease findings and have intact skin and mucous in the test region assessed by the gynaecologist at all the relevant time points.
- Subjects reporting mild to moderate vaginal dryness and dyspareunia during sex (when not using lubricant) in the past 3 months as confirmed on the Verbal Rating Scale (VRS).
- Post-menopausal
- Female subject in post-menopausal phase defined as having amenorrhea (absence of menstruation) for at least 12 months.
- Female subject with premature menopause - surgical menopause or physiological menopause within the last 12 months or after having received chemotherapy.
Exclusion
- Female subject who is pregnant, breast-feeding or trying to conceive.
- Female subject who has previously experienced an irritant or allergic reaction to any personal lubricant, vaginal moisturiser or female hygiene product or known to suffer from any contact allergen and/or are allergic to the investigational product ingredients.
- Female subject has urinary, vaginal infection (fungal, bacterial) or sexually transmitted infection as diagnosed by the investigator.
- Female subject presenting signs of internal irritation, active psoriasis, eczema or other active skin disorder or with a history of skin disorder
- Female subject presenting clinically abnormal findings other than irritation during the physical examination that will affect study outcome.
- Female subject who has started, stopped or changed hormonal treatments (including contraceptives) during the previous 3 months prior to screening.
- Female subject who has used any kind of topical histamine and/or topical hormonal based product for local treatment of vaginal dryness in the past 3 months.
- Female subject with any medical conditions which in the opinion of the investigator could compromise the immune function.
- Female subject taking steroid preparations, immune-suppressive drugs or any other medication which in the opinion of the investigator may affect the test results.
- Female subject who has had any change to medication or treatment regimen for the treatment of diabetes mellitus during the previous 3 months prior to screening.
- Female subject that will be unable to comply fully with the study requirements or unable to tolerate the procedures.
- Female subject that have had a suspicion of malignancy or history of malignancy within the past 2 years.
- Female subject who has had surgical cervical excision or vaginal and/or vulvar procedures in the previous year.
- Female subject that has had a positive cervical screening examination for Human Papillomavirus (HPV) within the 3 years of the screening visit.
- Female subject currently being treated with systemic medications or medicines that act locally in the vaginal area.
- Female subject using vaginal douches and is unwilling to stop its use at least 2 weeks prior to screening and throughout the clinical investigation.
- Female subject has changed contraceptive medication within the past 3 months or intending to change contraceptive medications.
- Female subject has participated in another investigation within 3 months prior to screening.
- Subject who is an employee at the site or a partner or first-degree relative of the Investigator.
- Subject fails to satisfy the investigator of fitness to participate for any other reason.
- Post-Menopausal
Key Trial Info
Start Date :
March 1 2021
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
June 29 2021
Estimated Enrollment :
183 Patients enrolled
Trial Details
Trial ID
NCT04908124
Start Date
March 1 2021
End Date
June 29 2021
Last Update
July 2 2021
Active Locations (1)
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1
proDERM GmbH
Hamburg, Pinneberg, Germany, 22869