- Trials with a EudraCT protocol (7)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
7 result(s) found for: Lactobacillus Plantarum.
Displaying page 1 of 1.
EudraCT Number: 2018-003095-12 | Sponsor Protocol Number: LPP17630-C-018 | Start Date*: 2019-08-16 |
Sponsor Name:PROGE FARM SRL | ||
Full Title: An investigator-blinded, active controlled, randomized, two parallel group, multi-dose clinical trial to prove the non-inferior efficacy of Lactobacillus plantarum P 17630 100.000.000 CFU soft vagi... | ||
Medical condition: Patients with clinically symptomatic vulvovaginal candidiasis. The following symptoms will be evaluated: pruritus, discharge, pain, dryness will be done using a daily VAS scale. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: BG (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 (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2008-005244-16 | Sponsor Protocol Number: CDiffPrevTrial1 | Start Date*: 2009-06-26 | |||||||||||
Sponsor Name:Wrightington, Wigan and Leigh NHS Trust | |||||||||||||
Full Title: Probiotics for the prevention of Antibiotics associated diarrhoea and Clostridium difficile associated diarrhoea A multi-centre, double-blind, randomized placebo controlled trial | |||||||||||||
Medical condition: Prevention of Clostridium Difficile associated diarrhoea. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
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 (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022886-92 | Sponsor Protocol Number: MWJ20100512V2 | Start Date*: 2011-04-19 |
Sponsor Name:Nottingham University Hospital NHS Trust | ||
Full Title: The effect of probiotics on the incidence of spontaneous bacterial peritonitis in patients with cirrhosis and ascites. | ||
Medical condition: cirrhosis and hepatic failure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
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: 2005-004541-34 | Sponsor Protocol Number: 21092005 | Start Date*: 2006-02-14 |
Sponsor Name:South Manchester University Healthcare Trust | ||
Full Title: The Effect of Enteral Administration of Synbiotics Upon Infection Rates in Major Burns | ||
Medical condition: Major burn injuries: Thermal related trauma with burn injury involving significant proportions of the total body surface area, as defined by age: Adults (>=17 years old): >= 15% body surface area ... | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
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