Lacticaseibacillus Rhamnosus CA15 (DSM 33960) Strain as a New Driver in Restoring the Normal Vaginal Microbiota

Urinary Tract Infections Clinical Trial

Official title:

Lacticaseibacillus Rhamnosus CA15 (DSM 33960) Strain as a New Driver in Restoring the Normal Vaginal Microbiota: a Randomized, Double-blind, Placebo-controlled Clinical Trial

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05796921
• Other study ID #: 113/2022/PO
• Status: Recruiting
• Phase: N/A
• Start date: January 2, 2023
• Est. completion date: March 30, 2024

Study information

• Verified date: April 2023
• Source: Universita degli Studi di Catania
• Contact: Marco M Panella, Prof
• Phone: +390953781102
• Email: mpanella[@]unict.it
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The aim of the present randomized double-blind placebo-controlled trial is to evaluate the efficacy of a probiotic formulation, containing the probiotic strain Lacticaseibacillus rhamnosus CA15 (DSM 33960), in the treatment of vaginal dysbiosis in terms of: (i) modulation of the microbiota (increase of lactobacilli and decrease of pathogens), (ii) reduction of clinical signs of inflammation, (iii) improvement of quality of life.

Description:

The aim of the present randomized double-blind placebo-controlled study is to evaluate the ability of the potential probiotic Lacticaseibacillus rhamnosus CA15 (DSM 33960) strain, orally administrated, to balance the vaginal microbiota of women with vaginal dysbiosis. Two hundred women, with signs and symptoms of vaginal dysbiosis, are recruited and randomly allocated to receive oral capsules containing the L. rhamnosus CA15 (DSM 33960) strain or placebo once daily for 10 days. Clinical and microbiological parameters are evaluated in three scheduled appointments: at baseline (T0), 10 days after the start of the treatment (T1), and 30 days after the end of the treatment (T2). In addition, at baseline (T0) and 30 days after the end of the treatment (T2), the quality of life will be evaluated through a quality of life assessment questionnaire.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 200
• Est. completion date: March 30, 2024
• Est. primary completion date: December 29, 2023
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 18 Years to 48 Years

Eligibility

Inclusion Criteria:

• Presence of at least one vaginal sign or symptom (leucorrhoea, burning, itching, subjective vaginal discomfort);
• Presence of at least 3 Amsel criteria;
• Nugent score greater than 7;
• Lactobacillary grade greater than 2 (LBG) (according to Donders classification);
• Vaginal dysbiosis based on microbial cell count.

Exclusion Criteria:

• Presence of sexually transmitted diseases due to Chlamydia, Neisseria gonorrhoeae or Trichomonas vaginalis as well as specific cervico-vaginitis or severe vulvovaginal symptoms related to acute candidiasis;
• Clinically evident herpes simplex infection;
• Human papillomavirus or human immunodeficiency virus infections;
• Use of antibiotics, antifungals, probiotics, or immunosuppressants within the past four weeks;
• Use of vaginal contraceptives and any other physiological or pathological condition that could potentially interfere with the results of the study (e.g. pregnancy or breastfeeding, chronic diseases, neoplastic diseases, diabetes, genital tract hemorrhages);
• Enrollment in other programs that involve the administration of products that may affect the composition of the vaginal microbiota.

Related Conditions & MeSH terms

• Bacterial Vaginosis
• Urinary Tract Infections
• Vaginosis, Bacterial

Intervention

Dietary Supplement:
• Lacticaseibacillus rhamnosus CA15 (DSM 33960) probiotic strain
Patients allocated to the probiotic arm will take the dietary supplement, containing 15 billion of the Lacticaseibacillus rhamnosus CA15 (DSM 33960) probiotic strain, once a day for 10 consecutive days.
• placebo
Patients allocated to placebo arm will take placebo capsules once a day for 10 consecutive days.

Locations

Country	Name	City	State
Italy	University of Catania	Catania

Sponsors (2)

Lead Sponsor	Collaborator
Agnese Maria Chiara Rapisarda	ProBioEtna

Country where clinical trial is conducted

Italy, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Microbiota	Change in the composition of the vaginal microbiota (significant reduction of pathogens responsible for vaginal dysbiosis and concomitant increase in lactobacilli)	Baseline; end of the treatment (10 days); wash-out (3 months)
Primary	Symptomatology	Change of signs (leucorrhoea, vulvovaginal erythema/edema) and symptoms (vulvar discomfort, burning, itching) associated to vaginal dysbiosis. Clinical signs and symptoms will be evaluated through a severity score on a scale of 0 (absent or normal) to 3 (severe).	Baseline; end of the treatment (10 days); wash-out (3 months)
Primary	Sign	Absence of inflammation according to Amsel's criteria and Nugent score between 0 and 3	Baseline; end of the treatment (10 days); wash-out (3 months)
Secondary	Well-being	Change in the quality of life, based on the Short Form-36 (SF-36) questionnaire. Values ranging from 0 to 100 indicate worst and better outcomes, respectively.	Baseline; end of the treatment (10 days); wash-out (3 months)