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Effect and Safety of Oral Vancomycin in Primary Sclerosing Cholangitis Patients

Evaluation of Effectiveness and Safety of Oral Vancomycin in Treatment of Primary Sclerosing Cholangitis.

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02605213
Enrollment
30
Registered
2015-11-16
Start date
2015-09-30
Completion date
2016-02-29
Last updated
2015-11-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Primary Sclerosing Cholangitis

Brief summary

Primary sclerotic cholangitis (PSC) is an inflammatory process of sclerotic cholangitis that involves intra and extra hepatic biliary system. There is no curative treatment for this disorder. Supportive and conservative treatments are the most common therapies that used for this disease. Although treatments such as ursodeoxycholic acid (UDCA) are recommended in some situations but whereas a hypothesis is stimulatory effect of intestinal anaerobic bacteria such as cholestridium difficile as pathogenesıs of PSC, so use of antibiotics is recommended for treatment of these patients. Therefore according to the great role of anaerobic bacteria such as cholestridium difficile in pathogenesis, antibiotics such as metronidazole and vancomycin can be counted as recommended therapies in PSC. In addition some studies correlated this effect of vancomycin to its immunomudulatory effect the cause reduction of inflammation in biliary system. But with all this detail there is no finality about effectiveness of antibiotic therapy and accordingly in this study the investigators compare oral vancomycin effect versus placebo in primary sclerosing cholangitis patients. In this double blind clinical trial 30 primary sclerosing cholangitis patients that divided in two 15 persosns group with Block Randomization method. in this study one group receive 250 mg oral vancomycin every 6 hours and other group receive placebo. The study duration is 12 weeks . The baseline laboratory tests and 1 month and 3 months after treatment concept of; Alkaline phosphatase, ALT, AST, GGT and serum total bilirubin and clinical manifestations such as tiredness, itching and probable adverse effects such as hypotension accompanied by flushing,erythematous rash on face and upper body (red neck or red man syndrome), chills and drug fever, eosinophilia and reversible neutropenia.

Interventions

DRUGVancomycin

Vancomycin for treatment of primary sclerosing cholangitis

DRUGPlacebo

Placebo for control Group of primary sclerosing vhlangitis

Sponsors

Tehran University of Medical Sciences
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

1. primary sclerosing chollangitis diagnosis more than 3 months 2. inflammatory bowel disease with cholestasis diagnosis more than 3 months 3. confirmed RCPM 4. confirmed pathology of inflammatory bowel disease

Exclusion criteria

1. signs of uncompensated cirrhosis like: hepatic encephalopathy, esophageal varices bleeding 2. gastrointestinal cancer or hepatic cancer 3. immunosuppressive agent using for hepatic problem (not vancomycine hypersensitivity)

Design outcomes

Primary

MeasureTime frameDescription
comparison of laboratory data AST between baseline and after treatment12 weeksAST
comparison of laboratory data Alkalyne phosphatase between baseline and after treatment12 weeksAlkaline phosphatase
comparison of laboratory data ALT between baseline and after treatment12 weeksALT
baseline databaselineserum Albumin
comparison of laboratory data GGT between baseline and after treatment12 weeksGGT
comparison of laboratory data serum total bilirubin between baseline and after treatment12 weeksserum total bilirubin

Secondary

MeasureTime frameDescription
Number of participants with adverse events12 weeksclinical manifestations such as tiredness, itching and probable adverse effects such as hypotension accompanied by flushing,erythematous rash on face and upper body (red neck or red man syndrome), chills and drug fever, eosinophilia and reversible neutropenia.

Countries

Iran

Contacts

Primary ContactNaser Ebrahimi Daryani, Professor
nasere@yahoo.com+989121104517
Backup ContactZahra Azizi, MD
zahra.azizi1990@gmail.com+989121308409

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 11, 2026