VaginitisNCT04676503
Vaginal and Rectal Colonization of Lactobacillus Crispatus NTCVAG04 Following Oral Administration in Patients With History of Vaginitis/Vaginosis
A study testing BIOVAGINIL in people with Vaginitis and Vaginosis, run by NTC srl at 1 site in Italy.
Trial 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… Read more about this study
- Who is it for?
- Ages 18 years and older, women only
- What is being tested?
- BIOVAGINIL
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 20 participants
- Where
- 1 siteItaly
- Study dates
- 22 Nov 2019to 21 Jul 2020
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- Women only
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Female
- Age > 18 years
- History of vaginitis/vaginosis
- Informed consent
Who cannot join
- Pregnancy
- Breastfeeding
- Need for treatment of vaginitis/vaginosis with any antibiotic drug
Trial locations and contacts
1 site in 1 country.
Italy1 site
Azienda Ospedaliera Universitaria di Siena - Unità Operativa Semplice Ginecologia Endocrinologica Centro Sterilità di Coppia
Siena, SI, 53100
About this study
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.
Read the 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.
- Being tested
- BIOVAGINIL
- Medical subject headings
- Vaginitis, Vaginal Diseases
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
BIOVAGINILDietary supplement
Biovaginil is a notified food supplement formulated as 480 mg capsules. Each capsule contains Lactobacillus crispatus NTCVAG04 3 billion and Vitamin A 120 μg.
| Study group | Role | What they receive |
|---|---|---|
| Test Arm - Biovaginil 480 mg capsules | Experimental | All patients will be treated with 1 capsule/day of BIOVAGINIL for two treatment cycles of 14 days each. Receives: Dietary Supplement: BIOVAGINIL |
What is being measured
The primary outcome is the main question the study is designed to answer.
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
Measured: 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)
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
Measured: At the end of the second treatment cycles (the cycle is 14 days - Visit 3 - 14th day (± 2) of the next menstrual cycle)
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
Measured: 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
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
Measured: At the end of the second treatment cycles (the cycle is 14 days - Visit 3 - 14th day (± 2) of the next menstrual cycle)
Secondary outcomes (1)
Number of patients with adverse events
Analysis of patients that reported an adverse events and analysis of number and type of adverse events.
Measured: up to 30 days
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted21 Dec 2020
- Study start22 Nov 2019
- Primary completion27 May 2020
- Study completion21 Jul 2020
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for VaginitisStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Model description
- Open-label pilot study
- Masking
- None (open label)
- Enrolment
- 20 participants (actual)
Sponsor and investigators
- Lead sponsor
- NTC srl
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Vincenzo De Leo, Principal investigator, Ospedale Santa Maria alle Scotte
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04676503
- Sponsor's protocol ID
- NTCVAG04_02-2018
- Status last verified
- Dec 2020
- First submitted
- 15 Dec 2020
- Last updated
- 21 Dec 2020
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 21 Dec 2020. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Vaginal and Rectal Colonization of Lactobacillus Crispatus NTCVAG04 Following Oral Administration in Patients With History of Vaginitis/Vaginosis
- ClinicalTrials.gov ID
- NCT04676503
- Acronym / sponsor ID
- NTCVAG04_02-2018
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 20 participants (actual)
- Lead sponsor
- NTC srlIndustry (pharma, biotech, devices)
- Study start
- 22 Nov 2019 (actual)
- Primary completion
- 27 May 2020 (actual)
- Study completion
- 21 Jul 2020 (actual)
- First posted
- 21 Dec 2020 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
- Model description
- Open-label pilot study
| Arm | Type | Receives |
|---|---|---|
| Test Arm - Biovaginil 480 mg capsules | Experimental | Dietary Supplement: BIOVAGINILAll patients will be treated with 1 capsule/day of BIOVAGINIL for two treatment cycles of 14 days each. |
Who may qualify
- Ages
- 18 years and older
- Sex
- Female only
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (4 listed)
- Female
- Age > 18 years
- History of vaginitis/vaginosis
- Informed consent
Key exclusion criteria (3 listed)
- Pregnancy
- Breastfeeding
- Need for treatment of vaginitis/vaginosis with any antibiotic drug
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| BIOVAGINILBiovaginil is a notified food supplement formulated as 480 mg capsules. Each capsule contains Lactobacillus crispatus NTCVAG04 3 billion and Vitamin A 120 μg. | Dietary supplement | Test Arm - Biovaginil 480 mg capsules |
Primary outcome
Positivity for NTCVAG04 in rectal swabs collected at the end of the first treatment cycle.
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)
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.
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)
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.
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
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.
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)
A descriptive statistical analysis will be performed for the vaginal swabs for NTCVAG04
1 secondary outcome
Number of patients with adverse events
Time frame: up to 30 days
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 21 Dec 2020.
Related trials for Vaginitis
Enrolling by invitationObservational study
Prevention of Vaginal Cuff Infection After Hysterectomy by Addition of Vaginal Clindamycin
Surgical Site Infection, Vaginal Cuff Cellulitis
Not yet recruitingPhase 2
WST03 Capsule Combined With Metronidazole for Bacterial Vaginosis
Bacterial Vaginosis (BV)
RecruitingPhase 1
A Randomized, Multicenter, Open-label, Active-controlled Phase Ib Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of Multiple Intravaginal Doses of GenSci142 in Patients With Bacterial Vaginosis (BV)
Randomized, Open-label
Not yet recruitingPhase 1
A Study to Test New Investigational Drugs (LCFA-01and LC103) for Bacterial Vaginosis (BV) Treatment
Bacterial Vaginosis
Recruiting
Multi-Gyn ActiGel Plus for Treatment of Bacterial Vaginosis
Bacterial Vaginoses
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Vincenzo De Leo principal investigator
Ospedale Santa Maria alle Scotte
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing BIOVAGINIL in people with Vaginitis and Vaginosis, run by NTC srl at 1 site in Italy.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 21 Dec 2020. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Italy. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Positivity for NTCVAG04 in rectal swabs collected at the end of the first treatment cycle. (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)). The study lists 4 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 21 Dec 2020.