Influence of Probiotics on the Vaginal Microbiota

Sponsor
Kinderwunsch Institut GmbH (Other)
Overall Status
Completed
CT.gov ID
NCT04471116
Collaborator
Institut AllergoSan (Other)
80
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2
19.4
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Study Details

Study Description

Brief Summary

The study aims to assess the influence of a probiotic supplement (OMNi-BiOTiC® FLORA plus +) on the vaginal microbiome composition of women suffering from infertility.

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: OMNi-BiOTiC® FLORA plus+
N/A

Detailed Description

Infertility is a global phenomenon affecting around 186 millions of people worldwide. Many circumstances have been identified to cause infertile conditions, with age being one of the most limiting factors. However, in recent years the microbiome has gained importance in the treatment of infertility and is considered as another important player to improve success rate of reproductive medicine treatments like in-vitro-fertilization (IVF).

Within the female reproductive tract the dominance of Lactobacilli is associated with a healthy vaginal microbial community in healthy reproductive-aged women. Since the microbiome has gained so much importance, its influence in IVF treatments is still controversially discussed. While some studies suggest a negative influence of vaginal dysbiosis on pregnancy rates a current meta-analysis showed no association between abnormal vaginal flora and conception rates following IVF treatment. One therapeutic approach is the administration of beneficial microorganisms (probiotics), mainly Lactobacillus species. The supplementation of exogenous lactobacilli strains has been suggested as cure for a dysbiotic vaginal flora to re-establish healthy conditions and improving female fertility health.

Hence, in the present study we wanted to investigate the impact of 4 probiotic strains (Lactobacillus crispatus LBV88, Lactobacillus rhamnosus LBV96, Lactobacillus gasseri LBV150N and Lactobacillus jensenii LBV116) on the relative abundance of vaginal microbiata species in women suffering from infertility.

80 infertile women suffering from infertility were included in the study within fertility treatment. 40 patients with IVF / ICSI were examined (20 with OMNi-BiOTiC® FLORA plus +, 20 as a control) and 40 patients with IUI / VZO (20 with OMNi-BiOTiC® FLORA plus +, 20 as a control). The control patients were selected from the routine patient collective of the Kinderwunsch Institut Schenk GmbH and receive no treatment with probiotics or placebo. Patients in the therapy group took 1 sachet of OMNi-BiOTiC® FLORA plus + (= 2 g) dissolved in 1/8 l of water once a day. Patients in the control group received no additional medication for routine treatment. Patients were randomized after inclusion in the study (block randomization).

On day 20 in the pre-cycle of hormonal stimulation, a vaginal smear sample was taken from the patient. The investigator introduced a sterile swab (eSwabTM, Copan Diagnostics Inc., USA), and took material from the mucosal surface. The eSwab was transferred to a sterile Falcon tube, stored at -72 ° C and then handed over to the company biovis Diagnostik MVZ GmbH (Germany) for 16s rRNA gene analysis. On day 20 in the stimulated cycle or subsequent cycle of the fertility treatment, another vaginal smear sample was taken and also stored in a sterile Falcon tube at -72 ° C.

The microbiota was determined using 16s rRNA gene analysis. The bacterial genomic DNA was isolated from the samples and the region V3-V4 was sequenced (Nextera XT, DNA Library Preparation Kit; Illumina MiSeq, Illumina, The Netherlands).

Study Design

Study Type:
Interventional
Actual Enrollment :
80 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
Influence of OMNi-BiOTiC® FLORA Plus+ on the Vaginal Microbiome of Patients Suffering From Infertility
Actual Study Start Date :
Mar 30, 2018
Actual Primary Completion Date :
Jul 19, 2019
Actual Study Completion Date :
Nov 12, 2019

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Therapy group

Patients in the therapy group took 1 sachet of OMNi-BiOTiC® FLORA plus + (= 2 g) dissolved in 1/8 l of water once a day

Dietary Supplement: OMNi-BiOTiC® FLORA plus+
OMNi-BiOTiC® FLORA plus + is a dietary supplement for the treatment of a disturbed vaginal flora (dysbiosis). The product combines probiotic bacterial strains with a special fiber mixture. The product contains the following strains: Lactobacillus crispatus LBV88, Lactobacillus rhamnosus LBV96, Lactobacillus gasseri LBV150N and Lactobacillus jensenii LBV116

No Intervention: Control group

Patients in the control group received no additional medication.

Outcome Measures

Primary Outcome Measures

  1. vaginal microbiome [1 month]

    The microbiota was determined using 16s rRNA gene analysis. The bacterial genomic DNA was isolated from the samples and the region V3-V4 was sequenced

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 40 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • patients with primary or secondary infertility

  • age between 18 and 40

  • signed informed consent

  • BMI between 19 and 29.9

Exclusion Criteria:
  • Patients with severe, acute and / or chronic diseases

  • obesity

  • hirsutism

  • current intake of antibiotics

  • State after hysterectomy

  • Simultaneous use of other probiotics

Contacts and Locations

Locations

Site City State Country Postal Code
1 Das Kinderwunsch Institut Schenk GmbH Dobl Styria Austria 8143

Sponsors and Collaborators

  • Kinderwunsch Institut GmbH
  • Institut AllergoSan

Investigators

  • Principal Investigator: Michael Schenk, MD, Kinderwunsch Institut GmbH

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Kinderwunsch Institut GmbH
ClinicalTrials.gov Identifier:
NCT04471116
Other Study ID Numbers:
  • FRED002
First Posted:
Jul 15, 2020
Last Update Posted:
Jul 16, 2020
Last Verified:
Jul 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Kinderwunsch Institut GmbH
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 16, 2020