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Vaginal and Rectal Colonization of Lactobacillus Crispatus NTCVAG04 Following Oral Administration in Patients With History of Vaginitis/Vaginosis

Primary Purpose

Vaginitis, Vaginosis

Status
Completed
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
BIOVAGINIL
Sponsored by
NTC srl
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Vaginitis

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Female
  • Age > 18 years
  • History of vaginitis/vaginosis
  • Informed consent

Exclusion Criteria:

  • Pregnancy
  • Breastfeeding
  • Need for treatment of vaginitis/vaginosis with any antibiotic drug

Sites / Locations

  • Azienda Ospedaliera Universitaria di Siena - Unità Operativa Semplice Ginecologia Endocrinologica Centro Sterilità di Coppia

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Test Arm - Biovaginil 480 mg capsules

Arm Description

All patients will be treated with 1 capsule/day of BIOVAGINIL for two treatment cycles of 14 days each.

Outcomes

Primary Outcome Measures

Positivity for NTCVAG04 in rectal swabs collected at the end of the first treatment cycle.
A descriptive statistical analysis will be performed for the rectal swabs for NTCVAG04
Positivity for NTCVAG04 in rectal swabs collected at the end of the second treatment cycle.
A descriptive statistical analysis will be performed for the rectal swabs for NTCVAG04
Positivity for NTCVAG04 in vaginal swabs collected at the end of the first treatment cycle.
A descriptive statistical analysis will be performed for the vaginal swabs for NTCVAG04
Positivity for NTCVAG04 in vaginal swabs collected at the end of the second treatment cycle.
A descriptive statistical analysis will be performed for the vaginal swabs for NTCVAG04

Secondary Outcome Measures

Number of patients with adverse events
Analysis of patients that reported an adverse events and analysis of number and type of adverse events.

Full Information

First Posted
December 15, 2020
Last Updated
December 18, 2020
Sponsor
NTC srl
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1. Study Identification

Unique Protocol Identification Number
NCT04676503
Brief Title
Vaginal and Rectal Colonization of Lactobacillus Crispatus NTCVAG04 Following Oral Administration in Patients With History of Vaginitis/Vaginosis
Official Title
Vaginal and Rectal Colonization of Lactobacillus Crispatus NTCVAG04 Following Oral Administration in Patients With History of Vaginitis/Vaginosis
Study Type
Interventional

2. Study Status

Record Verification Date
December 2020
Overall Recruitment Status
Completed
Study Start Date
November 22, 2019 (Actual)
Primary Completion Date
May 27, 2020 (Actual)
Study Completion Date
July 21, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
NTC srl

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to identify the presence of L. Crispatus in the rectum and vagina after oral administration of BIOVAGINIL by searching for specific DNA of the bacterial strain, to evaluate the tolerability of BIOVAGINIL and evaluate the minimum duration of the oral administration necessary to determine the appearance of L. Crispatus.
Detailed Description
In fertile, premenopausal healthy women, the vaginal ecosystem is dominated by Lactobacillus spp., but a diverse array of other bacteria can be present in much lower numbers. Over 120 species of Lactobacillus have been identified and more than 20 species have been detected in the vagina. Molecular-based techniques have demonstrated that healthy vaginal microflora does not contain high numbers of many different species of Lactobacillus. Rather, one or two lactobacilli from a range of three or four species (mainly L. crispatus and L. iners but also L. jensenii and L. gasseri) are dominant, whereas other species are rare, lower in titer and tend to be novel phylotypes. Vaginitis is defined as a spectrum of conditions that cause vaginal and sometimes vulvar symptoms such as itching, burning, irritation, odor and vaginal discharge. Infection is the most common cause of vaginitis, including bacterial vaginosis (BV), vulvovaginal candidiasis and trichomoniasis. Bacterial vaginosis is a very common microbiological disturbance of the vaginal environment in adult women and is characterized by a depletion of lactobacilli in favor of an overgrowth of anaerobic bacteria. Colonization by L. crispatus or L. jensenii is associated with a lower frequency of bacterial vaginosis, and L. crispatus is strongly correlated with the absence of BV, low pH, negative whiff test, absence of clue cells and normal vaginal discharge. Although antibiotic treatment of BV is strongly recommended, attempts at improving the efficacy of therapy are still a matter of debate. In fact, antimicrobial treatment of urogenital infections is not always effective, and problems remain due to bacterial and yeast resistance, recurrent infections and side effects. Alternative remedies are thus of interest and many studies have provided evidence of the beneficial functions of the human microbiota and prompted the selection of bacterial strains with health-promoting capacities for the treatment of conditions in which the microbiota, or its optimal functioning, is altered. The rationale for the use of probiotics in women is based on the genitourinary regulatory role played by the healthy vaginal microbiota and the need for restoration of this microbial ecosystem after insult. Until today, the most common way of delivering probiotic lactobacilli was the administration of vaginal suppositories.However, this route will no longer be acceptable as products containing probiotics (live microorganisms) are not admissible as medical devices as per European Medical Device Regulation (EU) 2017/245. Oral administration therefore represents an alternative and more patient-friendly concept for the restitution of the normal vaginal microbiota. Indeed, several studies demonstrated the ability of rectal bacteria to move from the intestinal tract to the vagina. Moreover, it was recently demonstrated that the administration of a yoghurt containing Lactobacillus spp. including L.. crispatus in addition to antibiotic treatment may improve recovery rate and symptoms of BV and is well tolerated. It is therefore reasonable to suppose that the oral administration of a food supplement containing an adequate concentration of a strain of L. crispatus, one of the predominant species, in the vaginal microbiota in asymptomatic women, may promote the re-colonization of the vaginal environment. Since this species is so representative and crucial in maintaining a healthy vaginal environment, we believe that it is of utter importance to understand its activity to fully disclose its potential. The aim of this pilot study is to investigate the presence of Lactobacillus crispatus NTCVAG04 in the vagina after oral administration of BIOVAGINIL, a food supplement, as a precondition for the subsequent evaluation of the ability of NTCVAG04 to rebalance the local microbiota and promote healing and/or prevention of recurrences of vaginitis/vaginosis.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Vaginitis, Vaginosis

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Open-label pilot study
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Test Arm - Biovaginil 480 mg capsules
Arm Type
Experimental
Arm Description
All patients will be treated with 1 capsule/day of BIOVAGINIL for two treatment cycles of 14 days each.
Intervention Type
Dietary Supplement
Intervention Name(s)
BIOVAGINIL
Intervention Description
Biovaginil is a notified food supplement formulated as 480 mg capsules. Each capsule contains Lactobacillus crispatus NTCVAG04 3 billion and Vitamin A 120 μg.
Primary Outcome Measure Information:
Title
Positivity for NTCVAG04 in rectal swabs collected at the end of the first treatment cycle.
Description
A descriptive statistical analysis will be performed for the rectal swabs for NTCVAG04
Time Frame
At the end of the first cycle ( the cycle is 14 days - Visit 2 - 21st day (± 2) of the menstrual cycle in progress or following enrolment)
Title
Positivity for NTCVAG04 in rectal swabs collected at the end of the second treatment cycle.
Description
A descriptive statistical analysis will be performed for the rectal swabs for NTCVAG04
Time Frame
At the end of the second treatment cycles (the cycle is 14 days - Visit 3 - 14th day (± 2) of the next menstrual cycle)
Title
Positivity for NTCVAG04 in vaginal swabs collected at the end of the first treatment cycle.
Description
A descriptive statistical analysis will be performed for the vaginal swabs for NTCVAG04
Time Frame
At the end of the first cycle (the cycle is 14 days - Visit 2 - 21st day (± 2) of the menstrual cycle in progress) or following enrolment
Title
Positivity for NTCVAG04 in vaginal swabs collected at the end of the second treatment cycle.
Description
A descriptive statistical analysis will be performed for the vaginal swabs for NTCVAG04
Time Frame
At the end of the second treatment cycles (the cycle is 14 days - Visit 3 - 14th day (± 2) of the next menstrual cycle)
Secondary Outcome Measure Information:
Title
Number of patients with adverse events
Description
Analysis of patients that reported an adverse events and analysis of number and type of adverse events.
Time Frame
up to 30 days

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Female Age > 18 years History of vaginitis/vaginosis Informed consent Exclusion Criteria: Pregnancy Breastfeeding Need for treatment of vaginitis/vaginosis with any antibiotic drug
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Vincenzo De Leo
Organizational Affiliation
Ospedale Santa Maria alle Scotte
Official's Role
Principal Investigator
Facility Information:
Facility Name
Azienda Ospedaliera Universitaria di Siena - Unità Operativa Semplice Ginecologia Endocrinologica Centro Sterilità di Coppia
City
Siena
State/Province
SI
ZIP/Postal Code
53100
Country
Italy

12. IPD Sharing Statement

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Vaginal and Rectal Colonization of Lactobacillus Crispatus NTCVAG04 Following Oral Administration in Patients With History of Vaginitis/Vaginosis

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