Treatment of the Intermediate Vaginal Microbiota With Vaginal Lactobacillus Casei Rhamnosus to Improve Pregnancy Outcome (LCR35&PTD)

February 23, 2021 updated by: Associate Prof. Ljubomir Petricevic MD, Medical University of Vienna

Treatment of the Intermediate Vaginal Microbiota With Vaginal Probiotics Containing Lactobacillus Casei Rhamnosus (Lcr Regenerans) to Improve Pregnancy Outcomes

In the currently presented trial, investigators aim to evaluate the treatment of the intermediate vaginal microbiota during the first trimester of pregnancy with vaginal lactobacilli to restore the normal vaginal microbiota and therewith reduce the rate of PTD. All pregnant women between 10 + 0 (10 weeks plus 0 days) and 16 + 0 (16 weeks plus 0 days) gestational weeks in study group will be treated with vaginal Lactobacilli Capsules containing L. Casei rhamnosus LCR 35

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Despite recent achievements in perinatal care, the prevention of preterm delivery (PTD) remains a major challenge in modern obstetrics. Healthy vaginal flora, dominated by Lactobacillus species (spp.), plays an important role in the protection against genital infections, which are considered a frequent cause of PTD. Imbalances of the vaginal flora caused by a reduction in the proportion of Lactobacillus spp. can lead to an overgrowth of mixed anaerobic bacteria, which can ultimately result in bacterial vaginosis (BV). Since the effect of treating pregnant women with an abnormal vaginal flora was introduced, BV has gained interest and is now a well-known risk factor for ascending infections and subsequent PTD. However, the overall risk reduction of PTD through antibiotic treatment of an abnormal flora was disproved by large and well-designed studies in a general obstetrical population.

At present, little is known about the role of the intermediate vaginal flora, which can either be regarded as the transition from a healthy to an abnormal flora or as the transition from abnormal flora back to a healthy vaginal microbiota. The intermediate vaginal flora constitutes a highly heterogeneous group that may or may not include vaginal Lactobacillus spp. and that may or may not be characterised by the presence of anaerobic bacteria. In 2007, a meta-analysis reported that the presence of intermediate vaginal flora was not associated with PTD, late miscarriage, maternal or neonatal infection, or perinatal mortality. In contrast, an observational study by Hay et al.reported a high rate of late miscarriage (16-24 gestational weeks) in women with intermediate vaginal flora at an examination before 16 gestational weeks. Additionally, another study reported an association of PTD with partial BV, which is defined as streaks of BV flora in a smear that has areas of normal flora.

Latest research reported that there is an association between the intermediate vaginal flora and PTD. In one of our previous studies, intermediate flora was identified on the examined screening smears of 529/8421 (6.3%) women. In this group, 349/529 (66%) women had a Nugent score of 4, 94/529 (17.8%) had a Nugent score of 5, and 86/529 (16.2%) had a Nugent score of 6. In women with a Nugent score of 4, 232/349 (66.5%) women were assigned to the Lactobacilli group. The Non-Lactobacilli group consisted of 117/349 (33.5%) women with a Nugent score of 4 due to the total absence of any bacterial colonisation, including Lactobacillus spp. The preterm delivery rate was significantly lower in the Lactobacilli than in the Non-Lactobacilli group On follow-up smears, bacterial vaginosis rates were 9% in the Lactobacilli and 7.8% in the Non-Lactobacilli group. Hence, according to this retrospective study, the absence of vaginal Lactobacillus species and any bacterial colonisation increases the risks of preterm delivery and low birth weight in women with intermediate vaginal flora in early pregnancy.

In the currently presented trial, investigators aim to evaluate the treatment of the intermediate vaginal flora during the first trimester of pregnancy with vaginal lactobacilli to restore the normal vaginal microbiota and therewith reduce the rate of PTD.

At investigators Department, pregnancy care includes a prenatal consultation, where women registered for a planned delivery at our department between 10 + 0 (10 weeks plus 0 days) and 16 + 0 (16 weeks plus 0 days) gestational weeks. Women underwent routine screening for asymptomatic vaginal infections and characterization due to Nugent score. All women except those with a normal flora (Nugent score 0 to 3) will be asked to undergo a follow-up smear between 14 + 0 (14 weeks plus 0 days) and 22 + 0 (22 weeks plus 0 days) gestational weeks at our department. Vaginal smears will be obtained after vaginal fluid collection with sterile swabs from the lateral vaginal wall and posterior fornix vaginae. Both at first and control smear. All smears will be Gram-stained and microscopically analyzed by one of four biomedical laboratory assistants, specialized in gynecological cytopathology, at a laboratory that is certified according to DIN EN ISO 9001:2008. Nugent scores of 0 to 3 will be considered to indicate normal vaginal flora, 4 to 6 to indicate intermediate vaginal flora, and 7 to 10 to indicate BV.

The present study follows a prospective randomized observer-blinded mono-centric design. After obtaining the results of vaginal swab According to the Nugent scoring system, two groups will be assigned: (i) pregnant women with an intermediate vaginal flora and a Nugent score of 4 with vaginal lactobacilli (Control Group), versus (ii) pregnant women with an intermediate vaginal flora and a Nugent score of 4 without vaginal lactobacilli (Study Group).

Therapy will be assigned due to protocol. Each group will be divided in a study and control group. Patients of the study group will be treated with muco-adhesive slow release vaginal tablets containing 876,9 mg Lactobacillus casei rhamnosus (Lcr regenerans) in concentration of 107 CFU/ml (Groups A + C). The treatment duration will be 8 days with two tablets every 4th day. Patients of the control group will not undergo any treatment (Groups B + D). A vaginal control smear will be obtained 4-6 weeks following the first study visit.

The primary outcome parameter will be the recovery to the normal vaginal flora (Nugent score 0 to 3). Secondary outcome parameters will include (i) the gestational age at delivery, recorded as term delivery at or after 37 + 0 gestational weeks, (ii) the rate of PTD, defined as spontaneous delivery at or before 36 + 6 gestational weeks, due to preterm premature rupture of the membranes and/or preterm labor, (iii) neonatal birthweight, defined as a the weight at the time of delivery, and (iv) the rate of live birth, defined as the delivery or PTD of an infant that had an Apgar score at 1 minute of > 0.

Study Type

Interventional

Enrollment (Actual)

120

Phase

  • Phase 3

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Austria
      • Vienna, Austria, 1090
        • Department of Obstetrics and Gynecology, Medical University of Vienna

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 55 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Description

Inclusion Criteria:

  • Pregnant women 10th to 16th Week of gestation

Exclusion Criteria:

  • Vaginal Bleeding, Twins, vaginal infections, Antibiotics up to 4 weeks to randomisation

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: A Nugent 4 + Lactobacilli
Intermediate vaginal Flora Nugent 4 with Lactobacilli. Intervention with vaginal probiotics with 'Lactobacillus casei rhamnosus (Lcr 35 regenerans)
Drug: Lactobacillus casei rhamnosus (Lcr 35 regenerans)
Probiotic vaginal tablets vith active probiotic strains
Other Names:
  • Gynophilus
Active Comparator: B Nugent 4 + Lactobacilli
Intermediate vaginal Flora Nugent 4 with Lactobacilli, NO Intervention
Other: NO Intervention
NO Intervention
Other Names:
  • NO Medication
Experimental: C Nugent 4 NO Lactobacilli
Intermediate vaginal Flora Nugent 4 NO Lactobacilli, Intervention with vaginal probiotics, with 'Lactobacillus casei rhamnosus (Lcr 35 regenerans)
Drug: Lactobacillus casei rhamnosus (Lcr 35 regenerans)
Probiotic vaginal tablets vith active probiotic strains
Other Names:
  • Gynophilus
Active Comparator: D Nugent 4 NO Lactobacilli
Intermediate vaginal Flora Nugent 4 NO Lactobacilli, No Intervention
Other: NO Intervention
NO Intervention
Other Names:
  • NO Medication

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
the recovery to the normal vaginal microbiota (Nugent score 0 to 3).
Time Frame: 4 Weeks
4 Weeks

Secondary Outcome Measures

Outcome Measure
Time Frame
the gestational age at delivery, recorded as term delivery at or after 37 + 0 gestational weeks
Time Frame: 9 Months
9 Months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Medical University of Vienna

Investigators

  • Study Chair: Ljubomir Petricevic, Prof, Medical University Vienna

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 2, 2017

Primary Completion (Actual)

November 1, 2020

Study Completion (Actual)

December 30, 2020

Study Registration Dates

First Submitted

November 28, 2016

First Submitted That Met QC Criteria

November 28, 2016

First Posted (Estimate)

December 1, 2016

Study Record Updates

Last Update Posted (Actual)

February 24, 2021

Last Update Submitted That Met QC Criteria

February 23, 2021

Last Verified

August 1, 2018

More Information

Terms related to this study

Other Study ID Numbers

  • MUV 012017

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

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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