Evaluation of the Efficacy and Safety of A High Molecular Weight, Natural Hyaluronic Acid Vaginal Gel in Women With Genitourinary Syndrome of Menopause

Menopause Syndrome Clinical Trial

Official title:

Evaluation of the Efficacy and Safety of A High Molecular Weight, Natural Hyaluronic Acid Vaginal Gel in Women With Genitourinary Syndrome of Menopause

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05263102
• Other study ID #: HAN2014005-CT02
• Status: Completed
• Phase: N/A
• Start date: March 1, 2020
• Est. completion date: August 13, 2022

Study information

• Verified date: December 2022
• Source: HAN Biomedical Inc
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The aim of the study is to evaluate the safety and efficacy of the vaginal gel with HMW HA in women with genitourinary syndromes due to either menopause or other causes such as the patients after ovarian or breast cancer diagnosis and treatment.

Description:

It was recognized that GSM is likely to be underdiagnosed and undertreated9. The North American Menopause Society (NAMS) issued the treatment guideline of GSM in 2014 and encouraged the physicians and nurses to pursue menopausal women to check if they have genitourinary syndrome. GSM is considered a progressive condition in menopausal women, and the primary goal of treatment strategy is symptom relief. Options include lifestyle changes, non-hormonal, and hormonal treatments. Hormonal therapies include both topical and systemic approaches. However, many women reported that substantial concerns about the long-term safety of hormonal products.The patients are aware of the possible relationship between cancer, heart disease, stroke, and estrogen-based treatments10. For considering long-term treatment strategy, estrogen free products of vaginal lubricant or vaginal moisturizer are recommended as first line treatment for those with mild to moderate syndrome.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 80
• Est. completion date: August 13, 2022
• Est. primary completion date: August 13, 2022
• Accepts healthy volunteers: No
• Gender: Female
• Age group: N/A and older

Eligibility

1. Subjects who have the relevant syndromes of vulvovaginal atrophy, and who are

1. In the status of menopause (=12 months after the last menstrual cycle); or

2. FSH > 40 mIU/ml and estradiol level < 20 pg/ml; or

3. bilateral ovary resection; or

4. the patients, i.e. breast cancer patients, who completed cancer therapy

2. Subjects have self-identified at least one of mild to moderate or severe symptoms listed below that are the most bothersome to her.

1. Vaginal dryness

2. Vaginal and/or vulvar irritation/itching

3. Dysuria

4. Vaginal pain associated with sexual activity

5. Vaginal bleeding associated with sexual activity

3. Subjects are willing to comply with all aspects of the study and have signed informed consent form.

Exclusion Criteria:

1. Subjects have been diagnosed with cervical or vaginal malignant neoplasms

2. Subjects with abnormal undiagnostic genital bleeding

3. Subject with active vaginal infection

4. Subjects with vaginal pH value < 4.5

5. Subjects are under hormone replacement therapy within three months

6. Subjects are under phytoestrogen treatment within two month

7. Subjects use of vaginal douche, lubricant or moisturizer in one week

8. Subjects are hypersensitive to sodium hyaluronate, carrageenan

Related Conditions & MeSH terms

• Menopause Syndrome
• Syndrome

Intervention

Device:
• Vaginal Moisturizing Gel
All eligible subjects will received the Vaginal Moisturizing Gel twice per week, total in 8 weeks

Locations

Country	Name	City	State
Taiwan	Changhua Christian Hospital	Changhua city
Taiwan	China Medical University Hospital	Taichung
Taiwan	Chi Mei Medical Center	Tainan
Taiwan	National Taiwan University Hospital	Taipei

Sponsors (1)

Lead Sponsor	Collaborator
HAN Biomedical Inc

Country where clinical trial is conducted

Taiwan, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	pH value change	The change of the vaginal pH value	from baseline to week 8
Secondary	The Questionnaire of Genitourinary Syndromes of Menopause	The change of its severity is used to evaluate symptomatic improvement. The minimum value is 0 and maximum value is 3, where higher scores mean a worse outcome.	from baseline to week 8
Secondary	Vaginal maturation index (VMI)	The change of its value is used to evaluate the maturation of the vaginal epithelial cells	from baseline to week 8