Effect of Oral Probiotic Yeast on the Composition of the Vaginal Microbiota in Healthy Women

Lesaffre

Status: Completed

Conditions: Vaginal Health

Treatments: Dietary Supplement: Saccharomyces cerevisiae, dose 500; Dietary Supplement: Saccharomyces cerevisiae, dose 1000; Dietary Supplement: Placebo

Study type: Interventional

Funder types: Industry; Other

Identifiers

NCT03574844

2017-A02709-44

Details and patient eligibility

About

This study is designed to evaluate the impact of oral consumption of the probiotic yeast CNCM I-3856 on healthy vaginal microbiota

Enrollment: 60 patients

Sex: Female

Ages: 18 to 45 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Caucasian or Asian women,
• With regular menstrual cycles, assessed as 28 days ± 3 days,
• With a normal vaginal flora : Nugent score ≤ 3,
• With the same efficient contraception method since at least 3 months before the start of the study, and accepting to maintain this program over the study. Authorized contraception methods: hormonal contraception (pill, patch, implant and intrauterine device), tubal ligation, ESSURE system and copper intrauterine device (without hormone),
• Agreeing to keep unchanged her intimate hygiene rules during the all duration of the study (same stable intimate hygiene habits since at least 3 months before the start of the study),
• Good general and mental health compatible with the study participation and allowing to be followed in ambulatory way according to the investigator opinion: no clinically significant and relevant abnormalities of medical history or physical examination;
• Having stable life habits since at least 3 months and accepting to maintain them stable during the study (dietary habits, tobacco and alcohol consumptions, physical activity and sexual activity),
• Tobacco consumption ≤ 10 cigarettes per day,
• Able and willing to participate to the study by complying with the protocol procedures (especially concerning study product consumption and biological samples collections), as evidenced by her dated and signed informed consent form,
• Affiliated with a social security scheme,
• Agreeing to be registered on the national file of volunteers participating in biomedical research.

Exclusion criteria

• Having hypersensitivity history to one of the ingredients of the study products,

• Suffering from a metabolic disorder such as diabetes, uncontrolled thyroidal trouble or other uncontrolled metabolic disorder,

• Suffering from a severe chronic disease (e.g. cancer, renal failure, hepatic or biliary disorders ongoing, chronic inflammatory digestive disease, arthritis, chronic respiratory trouble, chronic gastro-intestinal disorder, cardiac disease, immunodeficiency...) or diseases found to be inconsistent with the conduct of the study by the investigator (controlled arterial hypertension accepted),

• Suffering from Sexually Transmitted Infection (STI) or Disease (STD) such as HIV (Human Immunodeficiency Virus), B and C hepatitis, HPV (Human PapillomaVirus), Chlamydia infection, syphilis, gonorrhea, genital herpes, etc,

• Currently suffering or having suffer from bacterial, fungal, parasitic or viral infection of the uro-gynecological sphere (vaginitis, cystitis, cervix infection...), treated or not, in the 6 months previous to the study start,

• Having medical history or current pathology which could affect the study results or expose the subject to an additional risk according to the investigator,

• Currently pregnant, or lactating, intending to be pregnant within 2 months ahead or pregnancy and/or breastfeeding finished since less than 3 months,

• Ongoing symptoms of vaginal and/or urinary infection (belong to symptoms questionnaire) at the moment of the V0 and V1 visits,

• Recent history of radiotherapy (less than 6 months),

• Menopausal or pre-menopausal,

• With menstruation which usually lasts more than 7 days,

• Under chronic treatment with corticosteroids and/or immune modulator (immunostimulant, immunosuppressant...) or last intake within 3 months before the start of the study,

• Currently under medication or dietary supplement, oral or local, which could affect study parameters: antibiotic, antifungal, probiotic, prebiotic, symbiotic, phytoestrogens, etc, or stopped within a too short time window before study start (less than 4 weeks) ,

  .- Having a lifestyle deemed incompatible with the study according to the investigator (specific diet (vegetarian, vegan, hypocolaric...), alcohol consumption > 2 glasses / day, physical activity > 10 hours / week...),

• With a personal history of anorexia nervosa, bulimia or significant eating disorders according to the investigator,

• Planning to travel for a long time during the study duration or not able to be contacted for emergency reason during the study available,

• Presenting a psychological or linguistic incapacity to understand and sign the informed consent,

• Participating in another clinical trial or in exclusion period from a previous clinical trial,

• Having received, during the last 12 months, countervailing indemnities for clinical trial higher or equal to 4500 Euros,

• Under legal protection (guardianship, wardship) or deprived from her rights following judicial or administrative decision.

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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60 participants in 3 patient groups, including a placebo group

Saccharomyces cerevisiae, dose 500

Experimental group

Description:

Saccharomyces cerevisiae CNCM I-3856, 500 mg per day (2 capsules), for 4 weeks

Treatment:

Dietary Supplement: Saccharomyces cerevisiae, dose 500

Saccharomyces cerevisiae, dose 1000

Experimental group

Description:

Saccharomyces cerevisiae CNCM I-3856, 1 g per day (2 capsules), for 4 weeks

Treatment:

Dietary Supplement: Saccharomyces cerevisiae, dose 1000

Placebo

Placebo Comparator group

Description:

Maize starch and magnesium stearate, 1 g per day (2 capsules), for 4 weeks

Treatment:

Dietary Supplement: Placebo