Skip to main content
OpenTrials
Completed

NCT Number: NCT05263102

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

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.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Changhua Christian Hospital, Changhua, Taiwan

Loading trial locations.

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

  • Subjects who have the relevant syndromes of vulvovaginal atrophy, and who are
  • In the status of menopause (≥12 months after the last menstrual cycle); or
  • FSH > 40 mIU/ml and estradiol level < 20 pg/ml; or
  • bilateral ovary resection; or
  • the patients, i.e. breast cancer patients, who completed cancer therapy
  • Subjects have self-identified at least one of mild to moderate or severe symptoms listed below that are the most bothersome to her.
  • Vaginal dryness
  • Vaginal and/or vulvar irritation/itching
  • Dysuria
  • Vaginal pain associated with sexual activity
  • Vaginal bleeding associated with sexual activity
  • Subjects are willing to comply with all aspects of the study and have signed informed consent form.

Exclusion criteria

  • Subjects have been diagnosed with cervical or vaginal malignant neoplasms
  • Subjects with abnormal undiagnostic genital bleeding
  • Subject with active vaginal infection
  • Subjects with vaginal pH value < 4.5
  • Subjects are under hormone replacement therapy within three months
  • Subjects are under phytoestrogen treatment within two month
  • Subjects use of vaginal douche, lubricant or moisturizer in one week
  • Subjects are hypersensitive to sodium hyaluronate, carrageenan

Treatment and study plan

Vaginal Moisturizing Gel

Device

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

Primary outcomes

  1. pH value change

    Time frame: from baseline to week 8

    The change of the vaginal pH value

Secondary outcomes

  1. The Questionnaire of Genitourinary Syndromes of Menopause

    Time frame: from baseline to week 8

    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.

  2. Vaginal maturation index (VMI)

    Time frame: from baseline to week 8

    The change of its value is used to evaluate the maturation of the vaginal epithelial cells

Sponsors and collaborators

Lead sponsor

HAN Biomedical Inc

Industry

Registry information

Important dates

Study start
2020
Primary completion
2022
Study completion
2022
First posted
Mar 2, 2022
Registry last updated
Jan 3, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.