Expired Study
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Des Moines, Iowa 50314


Purpose:

The study will investigate whether probiotics given just before and shortly after major abdominal operation improve outcomes.


Study summary:

Perioperative probiotic intervention is associated with approximately 30% reduction of primary outcome measure.


Criteria:

Inclusion Criteria: - All elective major GI surgical patients Exclusion Criteria: - • Current episode of acute pancreatitis as defined by clinician - Active medication-induced immunosuppression including systemic corticosteroids, chemotherapy within 4 weeks, immunomodulating agents with transplant indication, biologicals for rheumatoid arthritis and inflammatory bowel disease. Topical chemotherapy or corticosteroids, and chemotherapy applied during operation are allowed.


NCT ID:

NCT01970683


Primary Contact:

N/A


Backup Contact:

N/A


Location Contact:

Des Moines, Iowa 50314
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: March 16, 2018

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