Drugs / Bifidobacterium infantis

Trials 3

PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 11 trial
Phase 1 NCT06793514 Feb → May 2025 overdue dry eye syndrome Mohsen Pourazizi Not yet recruiting No outcome recorded
Phase 41 trial
Phase 4 NCT05687409 Nov 2019 → May 2021 cirrhosis of liver, metagonimiasis First Affiliated Hospital of Zhejiang University Completed No outcome recorded
Phase not applicable1 trial
— NCT03644966 Jul 2018 → Dec 2022 bacterial infectious disease, urinary tract infection Ochsner Health System Completed No outcome recorded
Comparator or background therapy2 trials
Phase 3 NCT01340469 Comparator Jan 2005 → Mar 2008 necrotizing enterocolitis, nosocomial infection King Chulalongkorn Memorial Hospital Completed No outcome recorded
Phase 4 NCT01641341 Comparator Nov 2010 → Mar 2012 irritable bowel syndrome American Academy of Family Physicians Completed No outcome recorded

Evidence & citations 4 cited values

Every value below carries the sentence it was read from. 5 sources stand behind the page.

FieldValueCited text
Known as Bifidobacterium infantis “The experimental group will receive the oral probiotics (Lactobacillus casei, Lactobacillus rhamnosus, Lactobacillus acidophilus, Lactobacillus bulgaricus, Bifidobacterium...” NCT06793514 ↗
3

“Daily enteral probiotic supplementation (live Lactobacillus acidophilus and Bifidobacterium infantis) at a dose of 2.5 x 108 CFU of each strain once a day.” NCT01340469 ↗

“Dietary Supplement: Bifidobacterium infantis” NCT03644966 ↗

NCT01641341 ↗

Known as Bifidobacterium longum infantis “A 10-g packet of lactulose oral solution and three capsules of probiotics (each containing \> 4.2×106 CFU Clostridium butyricum and \> 4.2×105 CFU Bifidobacterium longum infantis).” NCT05687409 ↗
Modality Other / unclassified “live Lactobacillus acidophilus and Bifidobacterium infantis” NCT01340469 ↗
Route Other “Daily enteral probiotic supplementation” NCT01340469 ↗