EIC01-PMCF: Non-Interventional Multicentre Post-market Study of Ectoin® Vaginal Gel for Symptomatic Treatment of Vaginal Atrophy
Study Details
Study Description
Brief Summary
The goal of this multi-centre, prospective, open label, single arm, observational post-market clinical follow-up study (§23b of the MPG (German Medical Act) MDD 93/42/EEC and ISO14155:2020) is to investigate and evaluate the clinical efficacy of Ectoin® Vaginal gel (EIC01) to retain/restore the natural moisturization in the vaginal lumen and to alleviate vaginal atrophy symptoms.
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Detailed Description
A multi-centre, prospective, open label, single arm, observational post-market clinical follow-up study according to §23b of the MPG (German Medical Act) and conforming to MDD 93/42/EEC and ISO14155:2020.
Study participation will be offered to patients with symptoms of vaginal atrophy for which Ectoin® Vaginal Gel is indicated. Screening period might take up to 14 days. If the patient, at the screening visit, complies with all the inclusion criteria (except inclusion criterion No. 4 which is to be confirmed at the Baseline Visit) and she has signed the informed consent, she will be enrolled, and baseline visit will be performed on the same day.
The Ectoin® Vaginal Gel will be used for 20 days and in accordance with the IFU . Visits are scheduled on day 1, 5, and 20, at which the treatment is ended (End of treatment - EoT). Follow-up (FU) visit is planned on Day 23. Patient will record her symptoms and number of applied doses in the patient diary on daily basis, preferably around a specific time which has to be followed throughout the entire study period. Overall, participation will take at least 23 (+2) days and 37 (+2) days at maximum. The enrolment period will take 2 months. The total duration of the study is expected to be approximately 3-6 months.
The efficacy and safety of Ectoin® Vaginal Gel (EIC01) in the alleviation of vaginal atrophy symptoms will be evaluated in this study. Efficacy will be evaluated based on the improvement of Vaginal Atrophy symptoms at post-treatment measurements as compared to baseline values.
Primary endpoint is to evaluate the efficacy of the EIC01 product by analysing the difference in the sum scores of Vaginal Health Index (VHI) indicating both subjective and objective improvement in the vaginal atrophy condition after multiple application.
Secondary Endpoint:
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Improvement in individual and sum score of VAS for vaginal atrophy symptoms (feeling of dryness, itching, burning, pain during sexual intercourse) after single (immediate effect) and multiple applications
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Assessment of vaginal atrophy impact on life through Q/A
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Assessment of product acceptance and overall satisfaction through Q/A (on 20 day - V2) • Long-term treatment effect based on rate of improvement compared to baseline condition determined by subjective and objective assessments (5 days, 20 days and 23 days).
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Long-lasting effect assessed during follow-up by subjective and objective assessments on day 23.
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The treatment safety will be assessed by observation and documentation of adverse events and device deficiencies.
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Local tolerability will be assessed both by physician and patient using five-point scale (excellent, good, moderate, poor, bad).
Study Design
Outcome Measures
Primary Outcome Measures
- Change in Vaginal Health Index (VHI) Score [treatment 20 days + FU 3 to 5 days]
Assessment of vaginal lumen condition by gynaecologist from baseline to end of study on 20th day of application and thereafter, follow-up assessment in 3-5 days from end of treatment. The VHI components are graded from 1-5; where 1 indicating worst possible and 5 indicating best possible conditions.
Secondary Outcome Measures
- Change in vaginal pH [20+ (3-5) days FU]
Descriptive account of the vaginal pH as determined by the investigator during the visits using pH indicator strips of range 4.0 -7.0 pH
- Change in severity of VA symptoms (vaginal irritation, itching, vaginal dryness, and dyspareunia) [20+ (3-5) days FU]
Patient reported outcome on a VAS scare graded from 0-10; 0 = no problem and 10 = extremely unbearable
- Change in total score in Quality of Life evaluation parameters [20+ (3-5) days FU]
MCQ (multiple choice questions) format to choose the answer that corresponds best to the patient's situation. Patient have to choose between 4 options defining varying state possible outcome relevant to each specific question.
- Change in score of overall vaginal atrophy condition [20+ (3-5) days FU]
Patient reported outcome on a VAS scare graded from 0-10; 0 = no problem and 10= extremely unbearable
- Change in score of symptoms based rating on need for treatment [20+ (3-5) days FU]
Patient reported outcome on a VAS scare graded from 0-10; 0 = no at all and 10 = extreme need
- Overall tolerability assessments [20 days]
tolerability assessments (investigator and/or patient) on a 5-point scale; 1 = excellent (no reaction), 2 = good (small reaction that spontaneously resolves), 3 = moderate (reaction tolerated with difficulty by the subject), 4 = poor (reaction needing interruption of treatment), 5 = bad (serious reaction)
- Number of AEs and assessment of intensity, causality and seriousness of Adverse Events [20 days]
The adverse events will be classified as non-serious adverse event or serious adverse event (SAE), the intensity will be graded as mild, moderate, severe, life threatening or fatal. The causality will be classified as definitely, probably, possibly, or not related and in case of none of the above should be defined as an unknown relationship.
Eligibility Criteria
Criteria
Inclusion Criteria:
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Menopausal women 50 years of age or older with no menstruation for at least 12 months.
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Self-reported vaginal atrophy symptoms and presence of all 4 common vaginal atrophy symptoms i.e., feeling of vaginal dryness, itching, burning sensation and dyspareunia.
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Sexually active women.
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Vaginal atrophy clinically confirmed through physical examination of vagina and vaginal pH; pH ≥ 5 and VHI ≤ 15.
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Patient who qualifies for Ectoin® Vaginal Gel treatment according to the approved indication and in physician's opinion the participant will benefit from this treatment.
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Signed informed consent.
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Willingness of the participants to actively participate in the study and to come to the scheduled visits.
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Willingness of the participants to continue the application of EIC01 in the test area throughout the course of the study and to avoid forbidden treatment.
Exclusion Criteria:
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Women reporting systemic post-menopausal symptoms (eg. hot flushes, sleep disturbances, slowed metabolism etc.) in addition to clinically confirmed vaginal atrophy.
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Women who had not performed a cervical cytology in the last year to rule out underlying critical condition.
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Vaginal infections (in past 8 weeks)
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Women taking systemic hormone replacement or pills within last 6 months.
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Patients with concomitant clinically important medical disease according to the investigator's opinion that might interfere with patient safety or evaluation of study results; that includes but not limited to endometrial hyperplasia or cancer; undiagnosed vaginal bleeding; liver or kidney disorder; thromboembolic disorders; cerebrovascular accident, stroke, or transient ischemic attack; myocardial infarction or ischemic heart disease; malignancy; endocrine disease or any clinically important abnormalities on (if any) screening physical examination, mammogram, electrocardiogram (ECG), or laboratory tests (indicative of any vaginal infection).
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Participation in any other clinical study within the last 4 weeks prior to the baseline visit.
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Previous incident or knowledge of possible hypersensitivity or allergic reactions to any of the components of EIC01.
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Previous treatment with other local non-hormonal moisturisers/hormonal products within 1 month or use of lubricants within 1 week prior to inclusion.
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Treatment with systemic medications for other non-related health condition which might impact the study results e.g. glucocorticosteroids, antibiotics etc. which has the potential to bring about change in vaginal environment.
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Medical or mental condition for which in the opinion of the physician, patient will not be able to fulfil questionnaires independently or to adhere to instructions and procedures in accordance with the study protocol
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
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| 1 | bitop AG | Dortmund | Nordrhein-Westfalen | Germany | 44263 |
Sponsors and Collaborators
- Bitop AG
Investigators
- Study Chair: Shatadal Sen, MSc., Project Manager (Medical Device Development)
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- btph-045-2020-EIC01