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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05871255
Other study ID # 6407
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 5, 2022
Est. completion date April 30, 2023

Study information

Verified date May 2023
Source Liaquat University of Medical & Health Sciences
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Genitourinary syndrome of menopause (GSM) is a chronic and progressive syndrome characterized by a collection of genital and urinary signs and symptoms secondary to the state of hypoestrogenism related to menopause.


Description:

The aim of this prospective observational study is to evaluate safety and efficacy of Zantogin® Gel (ZG) a class II medical device developed for intravaginal use in the treatment of signs and symptoms of post-menopausal vulvovaginal atrophy (VVA), in terms of improvement of objective parameters assessing vaginal health (Vaginal Health Index score) and subsequent patients' sexual quality of life (Female Sexual Distress Scale).


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date April 30, 2023
Est. primary completion date June 30, 2022
Accepts healthy volunteers
Gender Female
Age group 45 Years to 65 Years
Eligibility Inclusion Criteria: - Age between 45-65 years - Menopause and symptomatic vulvovaginal atrophy (VVA) (vaginal dryness, dyspareunia, vaginal irritation, vaginal itching, dysuria) - No previous treatment for VVA - Informed written consent signed Exclusion Criteria: - Pregnancy - Previous or concurrent neoplasms - Uncompensated concomitant diseases (i.e., diabetes, cardiac diseases) - Previous or concurrent Hormone replacement therapy (HRT) or radiotherapy or chemotherapy.

Study Design


Related Conditions & MeSH terms

  • Atrophy
  • Genitourinary Syndrome of Menopause

Intervention

Other:
Zantogin® Gel
Zantogin® Gel (ZG) is a multicomponent vaginal lubricant endowed with lenitive and anti-inflammatory properties, developed as class II medical device for the treatment of VVA.

Locations

Country Name City State
Italy Department of Maternal-Fetal Medicine at Policlinico Umberto Rome

Sponsors (2)

Lead Sponsor Collaborator
Dr. Amjad Khan University of Roma La Sapienza

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in vaginal health index score Scale score range is 5-25. The minimum 5 points core indicates severe vulvovaginal atrophy and the maximum total score of 25 points indicates no clinical signs of vulvovaginal atrophy. 5.5 months
Primary Change in Female Sexual Distress Scale (FSD) A score of =11 effectively discriminates between women with FSD and no FSD. 5.5 months
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