RecruitingPhase 1NCT02137668

Treating Primary Sclerosing Cholangitis and Biliary Atresia With Vancomycin

The Human Gastrointestinal Tract Microbiota in the Setting of Treating Primary Sclerosing Cholangitis and Biliary Atresia With Vancomycin


Sponsor

Sacramento Pediatric Gastroenterology

Enrollment

200 participants

Start Date

Jul 1, 2010

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this study is twofold. First, is to determine whether vancomycin is effective in the early treatment of Biliary Atresia (BA) and Primary Sclerosing Cholangitis (PSC), and if so, by what mechanism. Secondly, to characterize human intestinal microbial communities and their interactions with the host.


Eligibility

Min Age: 2 WeeksMax Age: 40 Years

Inclusion Criteria2

  • Persons who have primary sclerosing cholangitis, biliary atresia, a chronic intestinal disorder or who are undergoing upper or lower endoscopy.
  • Persons who have primary sclerosing cholangitis or biliary atresia who are good candidates for vancomycin therapy.

Exclusion Criteria2

  • Patients that have taken antibiotics and/or immunomodulators within the last 3 months will be excluded as this will alter the original bacterial flora.
  • Females who are pregnant may not participate.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DRUGOral Vancomycin

Oral Vancomycin is given to PSC or BA participants


Locations(1)

Sacramento Pediatric Gastroenterology

Sacramento, California, United States

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT02137668


Related Trials