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Antibiotic-associated Colitis clinical trials

View clinical trials related to Antibiotic-associated Colitis.

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NCT ID: NCT05622721 Recruiting - Clinical trials for Clostridium Difficile

REMBRANDT: REcovery of the MicroBiome fRom Antibiotics for Dental implanTs

Start date: May 30, 2022
Phase:
Study type: Observational

Antimicrobial therapy can lead to disruption of the gut microbiome and infection with Clostridioides difficile, a disease associated with high morbidity and mortality, particularly among the elderly. Drawing on observations that pet ownership and close contact with pets are protective against colonization with C. difficile and recurrence of C. difficile infection, the proposed study will test the hypothesis that microbiota that provide colonization resistance against C. difficile are shared between patients and their pets and that pet contact can mitigate antimicrobial-associated gut dysbiosis and the risk of C. difficile infection. This study will further define epidemiologic and pathophysiologic characteristics of C. difficile infection and gut microbiome dysbiosis that could enhance therapeutic options for these conditions, potentially through non-invasive interventions involving animal contact.

NCT ID: NCT00304889 Completed - Clinical trials for Pseudomembranous Colitis

Vancomycin vs. Nitazoxanide to Treat Recurrent C. Difficile Colitis

Start date: January 2006
Phase: Phase 3
Study type: Observational

The purpose of this study is to compare the outcome of treatment with nitazoxanide vs. vancomycin for diarrheal disease due to Clostridium difficile in patients who have failed previous treatment with metronidazole.

NCT ID: NCT00304876 Completed - Clinical trials for Pseudomembranous Colitis

Fecal Bacterial Flora in Clostridium Difficile-Associated Diarrhea

Start date: October 2005
Phase: N/A
Study type: Observational

The investigators propose to study intensively the bacteriology of feces in C. difficile associated diarrheal disease, using a variety of conventional and very up-to-date techniques.

NCT ID: NCT00304863 Withdrawn - Clinical trials for Pseudomembranous Colitis

Addition of Lactobacillus to Metronidazole in Treatment of CDAD

Start date: August 1, 2008
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether dietary supplementation with Lactobacillus GG will reduce the rate of failure or relapse following treatment of CDAD with metronidazole.

NCT ID: NCT00304408 Completed - Clinical trials for Pseudomembranous Colitis

Association Between Response to Treatment of C. Diff Colitis and Anti-C.Diff Toxin Antibody

Start date: January 2005
Phase: Phase 4
Study type: Observational

The purpose of this study is three fold: 1)To collect serum from patients with documented Clostridium difficile infection and test for the presence of antibody to C. difficile toxin at the start and at the end of therapy, and again if a relapse or recurrence occurs. 2)To collect stool samples for test of C. difficile toxin at similar time intervals. 3)To assay random serum samples from the VA lab in order to determine the rate of antibody to C. difficile toxin in our patient population.

NCT ID: NCT00304369 Completed - Clinical trials for Pseudomembranous Colitis

Response of Clostridium Difficile Infection to Metronidazole Therapy

Start date: June 2005
Phase: N/A
Study type: Observational

In this record review study, our objective is to determine the rates of cure, failure and relapse following treatment of C. difficile colitis with metronidazole.

NCT ID: NCT00034294 Completed - Clinical trials for Antibiotic-associated Diarrhea

A Study of GT160-246 Versus Vancomycin in Patients With Clostridium Difficile-Associated Diarrhea

Start date: February 2002
Phase: Phase 2
Study type: Interventional

Approximately 300 patients will be entered into this study taking place throughout the United States, Canada and the United Kingdom. This study aims to determine if an investigational drug is safe and effective for treating the symptoms of C. difficile-associated diarrhea and lowering the risk of repeat episodes of diarrhea. The investigational drug will be evaluated in comparison to current standard antibiotic treatment, so all patients will receive active medication. All study-related care is provided including doctor visits, physical exams, laboratory tests and study medication. Total length of participation is approximately 10 weeks.