Zinc Containing Vaginal Topical " Suppository "
Primary Purpose
Genitourinary Syndrome of Menopause
Status
Completed
Phase
Phase 1
Locations
Egypt
Study Type
Interventional
Intervention
Zinc
Sponsored by

About this trial
This is an interventional treatment trial for Genitourinary Syndrome of Menopause
Eligibility Criteria
Inclusion Criteria:
- presence of symptoms of vulvovaginal atrophy/GSM in postmenopausal women. including vaginal dryness, burning, itching, vagina pain and dyspareunia. To be defined as a postmenopausal woman.
individuals had to have at least 12 consecutive months of amenorrhea without any other obvious reason/or consistently elevated follicle-stimulating hormone blood levels of 30 mIU/mL or higher.
Exclusion Criteria:
- premenopausal state,
- local or systemic hormone therapy within the past six months
- vaginal infection at presentation
- cytological atypia
- prior radiation treatment
- history of breast, ovarian or other gynecological cancer
- pelvic organ prolapse > stage 2
- recent use (3 months) of any vaginal product or douching.
Sites / Locations
- Al-Azhar University Hospitals and Ashmoun central hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
Zinc Group
Plcebo Group
Arm Description
25 cases will be undergo treatment with active ingredient
25 cases will be undergo treatment with placebo
Outcomes
Primary Outcome Measures
The using of novel zinc-containing vaginal suppositories
Assessment of postmenopausal symptoms as dryness, burning, and irritation by Vaginal Health Index (VHI) score: elasticity, fluid secretion, pH and epithelial mucosa (integrity) and moisture components. Each component is scored on a scale of 1 (worst) to 5 (best). Lower scores indicate more severe atrophy. VHI was calculated at baseline and 2 weeks after the treatment.
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT05453227
Brief Title
Zinc Containing Vaginal Topical " Suppository "
Official Title
Zinc Containing Vaginal Topical " Suppository " in Improving Post Menopausal Genitourinary Syndrome: "Double Blind Controlled Study "
Study Type
Interventional
2. Study Status
Record Verification Date
October 2023
Overall Recruitment Status
Completed
Study Start Date
December 1, 2021 (Actual)
Primary Completion Date
December 1, 2022 (Actual)
Study Completion Date
December 30, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Egymedicalpedia
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The genitourinary syndrome of menopause (GSM) is a new term that describes various menopausal symptoms and signs associated with physical changes of the vulva, vagina, and lower urinary tract.
The GSM includes not only genital symptoms (dryness, burning, and irritation) and sexual symptoms (lack of lubrication, discomfort or pain, and impaired function), but also urinary symptoms (urgency, dysuria, and recurrent urinary tract infections [UTI])
Detailed Description
The terms vulvovaginal atrophy and atrophic vaginitis were widely used until recently, but they have been considered to be inadequate for referring to the constellation of symptoms and signs associated with the genitourinary system after menopause.
The term vulvovaginal atrophy mentions the vulva and vagina only, and these words are not used comfortably in general social discussion and in the media. The term atrophic vaginitis implies a state of inflammation or infection, which is not a primary component of menopausal changes. In addition, a limitation of the terms vulvovaginal atrophy and atrophic vaginitis is that they do not take into account the symptoms of the lower urinary tract, which are among the most important symptoms related to menopause.
Vulvovaginal atrophy (VVA) is a prevalent condition affecting many postmenopausal women.1 Up to 40% of postmenopausal women develop symptoms of VVA.
It is most often diagnosed by its symptoms, including vaginal dryness, burning, itching, vagina pain and dyspareunia. More recently these symptoms have been described as a syndrome: the genitourinary syndrome of menopause (GSM).
This new term describes various menopausal symptoms and signs including not only genital symptoms but sexual (pain) and urinary symptoms (dysuria, urgency) as well.
The pathophysiology of GSM/VVA can be explained by the decline in estrogen levels associated with diminished ovarian function and natural aging.
Traditionally the treatment options for GSM/VVA was vaginal estrogen supplementation but many women are either unable to or are afraid to use hormones. There are several non-hormonal treatment modalities for the management of VVA related symptoms, especially for one of the most bothersome symptoms of vaginal dryness.
The 2013 position statement of The North American Menopause Society indicates that the first-line therapies to alleviate symptoms of VVA should include non-hormonal vaginal lubricants and moisturizers as well as regular sexual activity.
Although there are numerous vaginal moisturizers and lubricants are commercially available only a few of those have been tested in clinical trials.
Previously the investigators showed the role of vaginal zinc supplementation on vaginal remodeling. The investigators showed that in human vaginal smooth muscle cells, zinc has a beneficial effect on the production of extracellular components produced by the muscle at 20 μM zinc tissue level, thereby increasing the amount of elastin production.
Earlier animal studies have shown that zinc plays an important role in the vaginal extracellular matrix (ECM) composition. When rats were kept on a zinc-lacking diet, the vaginal structure became similar to the menopausal vagina.With vaginal zinc replacement, the vaginal ECM could be regenerated with characteristics equivalent to juvenile rats .
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Genitourinary Syndrome of Menopause
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
50 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Zinc Group
Arm Type
Active Comparator
Arm Description
25 cases will be undergo treatment with active ingredient
Arm Title
Plcebo Group
Arm Type
Placebo Comparator
Arm Description
25 cases will be undergo treatment with placebo
Intervention Type
Drug
Intervention Name(s)
Zinc
Intervention Description
To test the effect of a novel zinc-containing vaginal topical on GSM/VVA symptoms.
Primary Outcome Measure Information:
Title
The using of novel zinc-containing vaginal suppositories
Description
Assessment of postmenopausal symptoms as dryness, burning, and irritation by Vaginal Health Index (VHI) score: elasticity, fluid secretion, pH and epithelial mucosa (integrity) and moisture components. Each component is scored on a scale of 1 (worst) to 5 (best). Lower scores indicate more severe atrophy. VHI was calculated at baseline and 2 weeks after the treatment.
Time Frame
From baseline to 2 weeks after using the zinc sulphate
10. Eligibility
Sex
Female
Gender Based
Yes
Minimum Age & Unit of Time
55 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
presence of symptoms of vulvovaginal atrophy/GSM in postmenopausal women. including vaginal dryness, burning, itching, vagina pain and dyspareunia. To be defined as a postmenopausal woman.
individuals had to have at least 12 consecutive months of amenorrhea without any other obvious reason/or consistently elevated follicle-stimulating hormone blood levels of 30 mIU/mL or higher.
Exclusion Criteria:
premenopausal state,
local or systemic hormone therapy within the past six months
vaginal infection at presentation
cytological atypia
prior radiation treatment
history of breast, ovarian or other gynecological cancer
pelvic organ prolapse > stage 2
recent use (3 months) of any vaginal product or douching.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Assem Anwar, Professor
Organizational Affiliation
Department of Obstetrics & Gynecology Faculty of Medicine for boys, Al-Azhar University
Official's Role
Study Chair
Facility Information:
Facility Name
Al-Azhar University Hospitals and Ashmoun central hospital
City
Cairo
State/Province
Elmenofia
Country
Egypt
12. IPD Sharing Statement
Plan to Share IPD
Undecided
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Zinc Containing Vaginal Topical " Suppository "
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