A Clinical Investigation Into the Effectiveness and Safety of Five Water Based Personal Lubricants.
NCT04908124 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 183
Last updated 2021-07-02
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.
Conditions
- Dyspareunia
- Vaginal Dryness
Interventions
- DEVICE
-
Lubricant A
Water-based lubricant, which is suitable for oral, anal and vaginal sexual intercourse. Approximately 3g of lubricant will be considered a single application.
- DEVICE
-
Lubricant B
Water-based lubricant, which is suitable for oral, anal and vaginal sexual intercourse. Approximately 3g of lubricant will be considered a single application.
- DEVICE
-
Lubricant C
Water-based lubricant, which is suitable for oral, anal and vaginal sexual intercourse. Approximately 3g of lubricant will be considered a single application.
- DEVICE
-
Lubricant D
Water-based lubricant, which is suitable for oral, anal and vaginal sexual intercourse. Approximately 3g of lubricant will be considered a single application.
- DEVICE
-
Lubricant E
Water-based lubricant, which is suitable for oral, anal and vaginal sexual intercourse. Approximately 3g of lubricant will be considered a single application.
Sponsors & Collaborators
-
proDERM GmbH
collaborator INDUSTRY -
Reckitt Benckiser Healthcare (UK) Limited
lead INDUSTRY
Principal Investigators
-
Kirstin Deuble-Bente, Dr. · proDERM GmbH
Study Design
- Allocation
- RANDOMIZED
- Purpose
- PREVENTION
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 65 Years
- Sex
- FEMALE
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2021-03-01
- Primary Completion
- 2021-06-29
- Completion
- 2021-06-29
Countries
- Germany
Study Locations
More Related Trials
-
Therapy to Prevent Sexual Pain in Breast Cancer Survivors
NCT01539317 ·Status: COMPLETED ·Phase: PHASE3
-
Efficacy of Non-ablative Radiofrequency Combined With Pelvic Floor Muscle Training for Genitourinary Syndrome of Menopause in Breast Cancer Survivors (RF-SGM)
NCT07034976 ·Status: RECRUITING ·Phase: NA
-
Observational Study in Real Life to Describe the Libicare® Effectiveness in Female Sexual Dysfunction.
NCT04124640 ·Status: COMPLETED
-
The Efficacy of Topical Vaginal Oxytocin Gel in Postmenopausal Women With Vulvovaginal Atrophy
NCT06514586 ·Status: NOT_YET_RECRUITING ·Phase: PHASE3
-
Efficacy and Safety of Ospemifene in the Treatment of Moderate to Severe Vaginal Dryness and Vaginal Pain Associated With Sexual Activity
NCT00729469 ·Status: COMPLETED ·Phase: PHASE3
-
A Clinical Study to Evaluate Ospemifene in the Treatment of Vulvar and Vaginal Atrophy in Postmenopausal Women
NCT00276094 ·Status: COMPLETED ·Phase: PHASE3
-
Evaluate the Efficacy, Safety and Tolerability of a Non-hormonal Intravaginal Gel in Postmenopausal Women With Symptoms of Vaginal Dryness.
NCT02571127 ·Status: UNKNOWN ·Phase: PHASE4
-
Changes to Vulva, Vestibule, Urethral Meatus and Vagina 20 Weeks Post Daily Prasterone in Women With Dyspareunia
NCT03568604 ·Status: COMPLETED ·Phase: PHASE4
-
Radicle Revive 24: A Study of Health and Wellness Products on Menopausal Health and Related Health Outcomes
NCT06749288 ·Status: COMPLETED ·Phase: NA
-
Study to Evaluate the Effectiveness and Safety of Libicare® in Women With Low Arousal and Sexual Desire Levels
NCT04188600 ·Status: WITHDRAWN ·Phase: NA
-
Study To Investigate Effect Of A New Drug (PF-00446687) In Post-Menopausal Women Who Suffer From Sexual Dysfunction.
NCT00479570 ·Status: COMPLETED ·Phase: PHASE2
-
Estradiol Vaginal Softgel Capsules in Treating Symptoms of Vulvar and Vaginal Atrophy in Postmenopausal Women
NCT02253173 ·Status: COMPLETED ·Phase: PHASE3
-
Examining Effects of Intrarosa in Women With Genitourinary Syndrome of Menopause/Vulvovaginal Atrophy
NCT03782480 ·Status: UNKNOWN ·Phase: PHASE3
-
Study Evaluating the Efficacy and Safety of Three Formulations of Ultra-low Dose Estriol Vaginal Gel (0.005%, 0.002%, 0.0008% Estriol Vaginal Gel) for the Treatment of Vaginal Dryness in Postmenopausal Women With Vulvovaginal Atrophy
NCT02967510 ·Status: COMPLETED ·Phase: PHASE2
-
Detrol Long Acting (LA) vs Estrace Vaginal Cream for the Treatment of Overactive Bladder Symptoms
NCT00465894 ·Status: COMPLETED ·Phase: NA
-
Study of Oxytocin to Treat Vaginal Atrophy in Postmenopausal Women
NCT01432470 ·Status: COMPLETED ·Phase: PHASE2
-
Efficacy and Safety of HYDEAL-D Vaginal Pessaries Application on the Treatment of Vaginal Atrophy in Post-menopause Women
NCT03557398 ·Status: COMPLETED ·Phase: NA
-
Changes in the Impact of Genitourinary Syndrome of Menopause With a Novel Nonhormonal Vulvovaginal Gel Assessed by PROMs.
NCT06962345 ·Status: RECRUITING ·Phase: NA
-
Preventing Sexual Dysfunction With Aromatase Inhibitors
NCT01603303 ·Status: COMPLETED ·Phase: PHASE2
-
Safety and Efficacy of LibiGel® for Treatment of Hypoactive Sexual Desire Disorder in Postmenopausal Women
NCT00612742 ·Status: COMPLETED ·Phase: PHASE3
-
Study to Evaluate Ospemifene in Patients With Moderate to Severe Vaginal Dryness Due to Menopause
NCT02638337 ·Status: COMPLETED ·Phase: PHASE3
-
Efficacy of CL25216 on Vasomotor Symptoms in Women During Perimenopause
NCT07112651 ·Status: RECRUITING ·Phase: NA
-
Efficacy of Vaginal 17β-Estradiol on the Urinary Storage Symptoms in Postmenopausal Women
NCT06508944 ·Status: COMPLETED ·Phase: PHASE4
-
Vulvoscopy Changes of the Vulva, Vestibule and Vagina With Daily Ospemifene in Women With Dyspareunia From VVA
NCT02784613 ·Status: COMPLETED ·Phase: PHASE4
-
Evaluation of the Acceptability and Efficacy of 10 Micrograms of Estradiol Vaginal Tablets vs Promestriene Vaginal Cream
NCT04232813 ·Status: COMPLETED ·Phase: PHASE3