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Treating Primary Sclerosing Cholangitis and Biliary Atresia With Vancomycin

S

Sacramento Pediatric Gastroenterology

Status and phase

Enrolling
Phase 1

Conditions

Primary Sclerosing Cholangitis
Biliary Atresia

Treatments

Drug: Oral Vancomycin

Study type

Interventional

Funder types

Other

Identifiers

NCT02137668
Davies 1

Details and patient eligibility

About

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.

Full description

Investigators hope to learn to characterize human intestinal microbial communities (microbiome: the collection or collectivity of microorganisms) using molecular methods, examine the mechanisms of interaction between host and microbiome using genomic approaches, and determine how the microbiome both preserves local health and promotes pathology. Investigation will focus on primary sclerosing cholangitis, biliary atresia, as well as states of health. The composition of the associated microbiome will be assessed based on ribosomal DNA and RNA sequences, and attention will be given to richness (diversity), evenness (relative abundance), and variation with respect to time, person, and anatomic niche. Host response at the adjacent mucosal surface will be assessed based on genome-wide gene expression patterns. In addition, changes in the metabolites of the blood will be analyzed.

To see if the antibiotic vancomycin, when used for the early treatment of Biliary Atresia (BA) and Primary Sclerosing Cholangitis (PSC) is effective treatment for these diseases. Investigators hope to learn what effect Vancomycin has on the bacteria that are present in stool, body fluid or intestinal tissue on someone who has BA and PSC and if so by what mechanism.

Enrollment

200 estimated patients

Sex

All

Ages

2 weeks to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 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 criteria

  • 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.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

200 participants in 1 patient group

Oral Vancomycin
Experimental group
Description:
Every participant with PSC or BA will received the same Arm of Oral Vancomycin
Treatment:
Drug: Oral Vancomycin

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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