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Antibiotic-associated Diarrhoea clinical trials

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NCT ID: NCT02626104 Completed - Clinical trials for Antibiotic Associated Diarrhoea

Bovine Lactoferrin and Antibiotic-associated Diarrhoea.

BLAAD
Start date: December 2015
Phase: Phase 2
Study type: Interventional

This prospective, randomized, parallel-group, double blind, single-center study is to be conducted in the Medical University of Warsaw Public Paediatric Teaching Hospital in following departments: Department of Paediatric Gastroenterology and Nutrition, Department of Paediatrics and Nephrology, Department of Pediatric Pneumonology and Allergy, Department of Pediatrics with Medical Assessment Unit, Admissions Department. It is planned to include a total of 156 children aged between 12 months to 18 years old receiving antibiotic therapy because of acute respiratory tract infection/or urinary tract infection. The children will be randomly assigned to receive 100 mg of bovine lactoferrin or placebo twice a day orally for the whole period of antibiotic therapy. The primary efficacy parameter is occurrence of diarrhea during the antibiotic therapy and two weeks after, defined as > 3 stools a day, a watery or loose stool with/or occurrence of blood in the stool.

NCT ID: NCT01596829 Terminated - Clinical trials for Antibiotic-associated Diarrhoea

Effect of Probiotic Formula on Reducing the Risk for Antibiotic-associated Diarrhoea

Start date: December 2012
Phase: Phase 2/Phase 3
Study type: Interventional

Antibiotic treatment disturbs the balance of the intestinal microbiota and predisposes to antibiotic associated diarrhea. Previous studies have shown that the risk of developing diarrhea during a course of antibiotics may be reduced by simultaneous consumption of probiotics. The aim of the present study is to assess the effect of a probiotic formula containing four strains on reducing the risk of antibiotic associated diarrhea.