Performance and Safety of MUCOGYNE® Ovule as a Moisturizer (MOVHYDA)

MOVHYDA (MUCO245) - Performance and Safety of MUCOGYNE® Ovule as a Moisturizer

The aim of this post-Market Clinical Follow-up (PMCF) study is to confirm the efficacy and safety of MUCOGYNE® Ovule in the maintainance of natural moisture of the vulvovaginal mucosa and in the compensation for any natural secretions deficiencies, when used in accordance with its approved labeling, in the context of vulvovaginal dryness.

Study Overview

• Status: Terminated
• Conditions: Vaginal Dryness
• Intervention / Treatment: Device: Mucogyne Ovule

• Study Type: Interventional
• Enrollment (Actual): 33
• Phase: Not Applicable

Contacts and Locations

Study Locations

• France
  • Nogent-sur-Marne, France, 94130
    • JEAN Christian's medical office
  • Orléans, France, 45100
    • Dr Ramez GHADRI's medical office
  • Rennes, France, 35000
    • Dr Raïssa APERANO-MAS's medical office

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Adult; Older Adult
• Accepts Healthy Volunteers: No

Description

Inclusion Criteria:

Women with the following conditions:

• ≥ 18 years of age at inclusion with vaginal dryness, irrespective of the cause (which may or may not be accompanied by irritation of the vulva, discomfort, or itchiness) : women who suffer pain during sexual intercourse, women taking the mini pill, mothers during breastfeeding, menopausal women and women taking anti-acne treatment.
• Having a Vaginal Health Index Score (VHIS) <15 associated to pain and/or dyspareunia feeling.
• If the patient has reproductive potential, she must be willing to use effective method of contraception (oral contraceptive, intrauterine device, subcutaneous contraceptive implant, vaginal ring, and condom).
• Patient agrees to not use any local oestrogens, or other vaginal product during the study
• Patient agrees to not modify their intimate hygiene and lubricant products
• Patient able to understand and sign the informed consent form before beginning any study procedure
• Patient able to comply with study requirements, as defined in the protocol.
• Patient affiliated to a health social security system.

Exclusion Criteria:

Women with the following conditions:

General criteria:

• Pregnant women (patient of childbearing potential must not be pregnant and must agree to avoid pregnancy during the study by using an effective birth control method from at least one month before D0 (V1) and throughout the duration of the study)
• Patient participating at the same time in another interventional trial within the four previous weeks and during the study period, being in an exclusion period for a previous study
• Patient deprived of freedom by administrative or legal decision or under guardianship
• Patient in a social or sanitary establishment
• Patient suspected to be non-compliant according to the investigator's judgment
• Patient in an emergency situation

Criteria related to patient's status:

• Patient with known hypersensitivity to one of MUCOGYNE® Ovule components
• Patient with a known vaginal pathology (clinical diagnosis only) other than vaginal dryness/atrophy

Criteria related to previous or ongoing treatments:

• Patient with a condition or receiving a medication which, in the investigator's judgment, put the patient at undue risk
• Patient suffering from systemic diseases and/or using concurrent therapy that may interfere with the evaluation of the study results

• Patient undergoing a topical treatment on the test area or a systemic treatment such as:

  • corticosteroids during the 2 previous weeks and during the study
  • retinoids and/or immunosuppressors during the 1.5 previous months and during the study
  • Patient having started or changed her oral contraceptive or any other hormonal treatment during the three previous months

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Other
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Mucogyne treatment; 2 planned visits for each eligible patient : Screening/Baseline visit : V1 at Day 0. Patient receive Mucogyne Ovule.; End-of-study visit : V2 at Day 35 ± 3	Device: Mucogyne Ovule; At inclusion visit (V0), the Investigator will ask the subject to use MUCOGYNE® Ovule 2 times a week until symptoms improve during 5 weeks (D35± 3) preferably at bedtime

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Assessment of the efficacy of MUCOGYNE® Ovule intra vaginal applications on subjects' vaginal dryness irrespective of the cause over a 35-day period of use	Primary efficacy criterion: Clinical scoring, by the investigator, of the Vaginal Health Index Score (VHIS), including evaluation of elasticity, fluid volume, pH, epithelial integrity, and moisture. The minimum score is 5 and the maximum score is 25. If VHIS <15, the vagina is considered atrophic.	Day 0 to Day 35 ± 3

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Assessment of the local performance of MUCOGYNE® Ovule in reducing vulva irritation	Secondary efficacy criteria : Auto-evaluation, by the subjects, of vulva irritation on Visual Analogical Scales (VAS) from 0 to 10	Day 0 to Day 35 ± 3
Assessment of the local performance of MUCOGYNE® Ovule in reducing vulvo-vaginal discomfort	Secondary efficacy criteria : Auto-evaluation, by the subjects, of discomfort on Visual Analogical Scales (VAS) from 0 to 10	Day 0 to Day 35 ± 3
Assessment of the local performance of MUCOGYNE® Ovule in reducing itching	Secondary efficacy criteria : Auto-evaluation, by the subjects, of itching on Visual Analogical Scales (VAS) from 0 to 10	Day 0 to Day 35 ± 3
Assessment of the local performance of MUCOGYNE® Ovule in reducing pain and/or dyspareunia related to vaginal dryness	Secondary efficacy criteria : Auto-evaluation, by the subjects, of pain and/or dyspareunia on Visual Analogical Scales (VAS) from 0 to 10	Day 0 to Day 35 ± 3
Assessment of the patient's sexual function	Secondary efficacy criteria : Completion of the self-reported FSFI (Female Sexual Function Index) to investigate sexual function (for women having sexual relations). The minimum score is 2 and the maximum score is 36. An alteration in sexuality is a score less than or equal to 26,55.	Day 0 to Day 35 ± 3
Assessment of the patient's satisfaction	Secondary efficacy criteria : Completion of the intra vaginal treatment satisfaction questionnaire (Likert questionnaire) to assess the level of satisfaction of the treatment on the vaginal symptoms. Two questions with 5 possible answers :; 1 : Strongly agree; 2 : Agree; 3 : Neither; 4 : Disagree; 5 : Strongly disagree	Day 0 to Day 35 ± 3
Assessment of changes in patient's clinical status	Secondary efficacy criteria :Completion of the Patients' Global Impression of Change (PGIC) Scale to assess the changes perceived by the patient following the treatment taken from 1 to 7. An improvement is a score from 1 to 3 whereas a deterioration is a score of 5 to 7. A score of 4 means stability.	Day 0 to Day 35 ± 3
Assessment by investigator of changes in patient's clinical status	Secondary efficacy criteria :Completion of the Clinical Global Impressions-Improvement (CGI-I) by the investigator to assess the changes following the treatment taken from 1 to 7. An improvement is a score from 1 to 3 whereas a deterioration is a score of 5 to 7. A score of 4 means stability.	Day 0 to Day 35 ± 3
Assessment of the safety of MUCOGYNE® Ovule	Secondary efficacy criteria : Reporting of number, nature and characteristics of any adverse event : incidence, seriousness, severity, resolution.	Day 0 to Day 35 ± 3
Assessment of the device deficiencies of MUCOGYNE® Ovule	Secondary efficacy criteria : Reporting of Device deficiencies: type of deficiency, batch number, action taken, consequence of deficiency.	Day 0 to Day 35 ± 3
Assessment of the usability of MUCOGYNE® Ovule	Secondary efficacy criteria : Completion of the usability question by the patient. There are 4 possible answers :; Very easy; Easy; Difficult; Very Difficult	Day 0 to Day 35 ± 3

Collaborators and Investigators

• Sponsor: Biocodex
• Collaborators: Voisin Consulting Life Science (VCLS)
• Investigators: Study Director: Oana BERNARD, MD, Chief Scientific officer

Study record dates

Study Major Dates

• Study Start (Actual): April 11, 2024
• Primary Completion (Actual): February 14, 2025
• Study Completion (Actual): February 14, 2025

Study Registration Dates

• First Submitted: February 1, 2024
• First Submitted That Met QC Criteria: February 20, 2024
• First Posted (Actual): February 28, 2024

Study Record Updates

• Last Update Posted (Actual): April 13, 2025
• Last Update Submitted That Met QC Criteria: April 10, 2025
• Last Verified: April 1, 2025

More Information

Terms related to this study

• Other Study ID Numbers: MUCO245; 2023-A02081-44 (Other Identifier: ID-RCB)

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No
• product manufactured in and exported from the U.S.: No