Evaluating the effectiveness of the traditional vaginal product on vulvovaginal atrophy

Phase 2

Recruiting

• Conditions: Vulvovaginal atrophy.; N95.2; Postmenopausal atrophic vaginitis

• Registration Number: IRCT20191210045687N1
• Lead Sponsor: Shahid Beheshti University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 24 February 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 50

Inclusion Criteria

Having a patient's consent to participate in the project
Ability to fill out forms and questionnaires alone or with the help of a researcher
18 years or older
Married
Menopause
History of breast cancer
Hormonal treatment history
Having subjective symptoms of vulvovaginal atrophy (itching, burning, dryness, dyspareunia) with a minimal sum score of 3

Exclusion Criteria

Having multiple sex partners
Acute psychiatric illness and antidepressant use during the last month
Other cancers at the same time as breast cancer
Incomplete chemotherapy and radiotherapy
Use of lubricant or vaginal moisturizer and other vaginal medications during the last month
Not having a negative Pap smear over the last year

Study & Design

• Study Type: interventional
• Study Design: Not specified