- Trials with a EudraCT protocol (13)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
13 result(s) found for: Lactobacillus rhamnosus.
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EudraCT Number: 2015-003944-38 | Sponsor Protocol Number: 15-PP-13 | Start Date*: 2016-04-19 |
Sponsor Name:CHU NICE | ||
Full Title: Treatment of the oral aphtose récidivante and idiopathique of the adult by probiotics Double-blind randomized interventional study versus placebo | ||
Medical condition: aphtous stoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-002376-41 | Sponsor Protocol Number: MICINT | Start Date*: 2018-09-10 | |||||||||||
Sponsor Name:Zealand University Hospital, Gynecological department | |||||||||||||
Full Title: Modulating the Vaginal Microbiome after Implantation Failure - A randomized placebo controlled study of lactobacilli supplements | |||||||||||||
Medical condition: Sub-optimal vaginal and/or endometrial microbiome. | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000228-20 | Sponsor Protocol Number: 16012020001 | Start Date*: 2020-08-28 |
Sponsor Name:Medical University of Graz | ||
Full Title: Probiotic dietary Intervention in Polycystic Ovary Syndrome – A Randomized Controlled Trial | ||
Medical condition: Polycystic Ovary Syndrome (PCOS) is a hormonal and metabolic disorder affecting up to 20 percent of women worldwide, depending on diagnostic criteria. A very common definition of PCOS based on the ... | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: AT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-005833-38 | Sponsor Protocol Number: LCR35_ESBL-01 | Start Date*: 2012-07-03 | |||||||||||
Sponsor Name:Medical University of Vienna | |||||||||||||
Full Title: Removal of intestinal colonization with multi resistant bacteria by ingestion of Lactobacillus casei rhamnosus LCR 35 | |||||||||||||
Medical condition: Intestinal colonisation with multiresistant bacteria | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002291-13 | Sponsor Protocol Number: DIALAGG | Start Date*: 2012-10-19 | |||||||||||
Sponsor Name:InfectoPharm - Arzneimittel und Consilium GmbH | |||||||||||||
Full Title: Multicentre, prospective, double-blind, two-armed, placebo-controlled phase III study to evaluate the efficacy and safety of the treatment of diarrhoea with Lactobacillus rhamnosus GG (InfectoDiarr... | |||||||||||||
Medical condition: Acute diarrhoea in infants and toddlers | |||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-005111-14 | Sponsor Protocol Number: HPE-4/LCR | Start Date*: 2019-04-25 |
Sponsor Name:Kepler Universitätsklinikum, Medcampus III, Klinik für Interne 2 | ||
Full Title: First-line Treatment of Helicobacter pylori with the Probiotic Lactobacillus casei rhamnosus LCR35 Alone or in Combination with a Levofloxacin-based Sequential Therapy: A Randomized, Placebo-contro... | ||
Medical condition: Helicobacter pylori infection | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2016-000371-24 | Sponsor Protocol Number: DOBO-01-16 | Start Date*: 2016-05-24 |
Sponsor Name:Laboratorios Ordesa | ||
Full Title: Multicenter pilot study for comparison of the efficacy of vaginal capsules with boric acid and L. gasseri and L. rhamnosus versus other vaginal drugs, in patients with bacterial or candida Vulvovag... | ||
Medical condition: Bacterial or candidiasic vulvovaginitis | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-019104-23 | Sponsor Protocol Number: Gastro CHU 09-1 | Start Date*: 2010-07-09 | |||||||||||
Sponsor Name:THT Research sprl | |||||||||||||
Full Title: Etude prospective de l'efficacité d'un mélange probiotique dans le syndrome du colon irritable. | |||||||||||||
Medical condition: Syndrome du colon irritable (irritable bowel syndrome) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-000913-30 | Sponsor Protocol Number: Nath1/2008 | Start Date*: 2008-10-13 | |||||||||||
Sponsor Name:NATHURA SRL | |||||||||||||
Full Title: A symbiotic for the treatment of functional constipation | |||||||||||||
Medical condition: Functional crhonic constipation | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000820-83 | Sponsor Protocol Number: NNL-2017 | Start Date*: 2017-07-03 | ||||||||||||||||
Sponsor Name:University of Oulu | ||||||||||||||||||
Full Title: Otitis Media and Nasopharyngeal Microbiome in Children. The change of nasopharyngeal microbiome and its role as a risk factor of otitis media. Streptococcus salivarius K12 and the change of nasop... | ||||||||||||||||||
Medical condition: We investigate role of microbiota as the risk factor of acute otitis media in children. | ||||||||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: FI (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-002823-27 | Sponsor Protocol Number: GAVALAGG | Start Date*: 2016-11-17 | |||||||||||
Sponsor Name:INFECTOPHARM Arzneimittel GmbH | |||||||||||||
Full Title: Placebo-kontrollierte, multizentrische, randomisierte, doppelblinde Phase III-Studie zur Verbesserung der gastrointestinalen Verträglichkeit einer per-oralen Antibiotikatherapie durch add-on-Gabe v... | |||||||||||||
Medical condition: Verbesserung der gastrointestinalen Verträglichkeit einer per-oralen Antibiotikatherapie | |||||||||||||
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Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000209-31 | Sponsor Protocol Number: LACTO2 | Start Date*: 2007-03-08 | |||||||||||
Sponsor Name:UNIVERSITA CAMPUS BIOMEDICO | |||||||||||||
Full Title: Efficacy of Lactobacillus Rhamnosus GG on preventing acute phases in patients affected by allergic conjunctivitis | |||||||||||||
Medical condition: allergic conjunctivitis | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-017901-12 | Sponsor Protocol Number: LYO_2009-09 | Start Date*: 2010-02-26 | |||||||||||
Sponsor Name:LYOCENTRE | |||||||||||||
Full Title: Etude de l’efficacité et de la tolérance du traitement par la culture totale lyophilisée de lactobacillus casei variété rhamnosus (Lcr35 Lc) administré par voie vaginale dans la prévention de réci... | |||||||||||||
Medical condition: vaginose bactérienne récidivante | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
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