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RECRUITING
NCT07154992
NA

Clinical Trial to Evaluate the Efficacy of Lacticaseibacillus Rhamnosus CRL1505 in the Prevention of Upper Respiratory Tract Infections in Children

Sponsor: Bioithas SL

View on ClinicalTrials.gov

Summary

Randomized, double-blind, placebo-controlled, parallel-group, clinical trial to assess the efficacy of the intake of a probiotic product composed of Lacticaseibacillus rhamnosus CRL1505 strain in reducing or preventing upper respiratory tract infections (URTIs) in a healthy paediatric population.

Official title: Randomized, Double-blind, Placebo-controlled Clinical Trial to Evaluate the Efficacy and Safety of Lacticaseibacillus Rhamnosus CRL1505 in the Prevention of Upper Respiratory Tract Infections in a Healthy Paediatric Population

Key Details

Gender

All

Age Range

3 Years - 12 Years

Study Type

INTERVENTIONAL

Enrollment

268

Start Date

2024-12-17

Completion Date

2027-04

Last Updated

2025-09-12

Healthy Volunteers

Yes

Interventions

DIETARY_SUPPLEMENT

Probiotic - Lacticaseibacillus rhamnosus CRL1505

The probiotic product is provided in 2g sticks containing the strain Lacticaseibacillus rhamnosus CRL1505 at a concentration of ≥ 1.0E+8 CFU/g, with corn starch and maltodextrin as excipients.

DIETARY_SUPPLEMENT

Placebo

The placebo product is provided in 2g sticks of corn starch and maltodextrin.

Locations (1)

MiBioPath Research Group (UCAM)

Murcia, Spain