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Clinical Trials/NCT03778918
NCT03778918
Unknown
Not Applicable

The Comparison Between That Expression Pattern and Disease Activity of Variable Biomarkers in Inflammatory Bowel Disease Patients and General Control Group. Multicenter, Prospective Study

Bo-In Lee1 site in 1 country200 target enrollmentAugust 1, 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Inflammatory Bowel Diseases
Sponsor
Bo-In Lee
Enrollment
200
Locations
1
Primary Endpoint
measurement of blood-based biomarkers to predict disease activity 1
Last Updated
6 years ago

Overview

Brief Summary

The aims of this study is to investigate a blood-based biomarker that can replace endoscopy in patients with inflammatory bowel disease. For this purpose, blood sample of patients wiht inflammatory bowel disease (ulcerative colitis, Crohn 's disease) was collected at the same time the endoscopy is performed, stored after centrifugation, and analyzed accordingly. Selected biomarkers from the blood sample were investigated to compare those of patients with inflammatory bowel disease and those of general controls. Males and females over the age of 19 participated in the study and are excluded if they have chronic kidney disease or blood clotting disease. The outcome is a find of a blood-based biomarker that best reflects a disease activity.

Detailed Description

Inflammatory bowel disease refers to chronic inflammation of the unknown origin that occurs in the intestine. It usually refers to ulcerative colitis and Crohn's disease, which are idiopathic inflammatory bowel diseases. While it had been known to be a common disease in the western world, in recent decades the incidence of ulcerative colitis and Crohn's disease has rapidly increased in Korea as well. Endoscopic examination is a gold standard in order to determine the activity of inflammatory bowel disease, but it is hardly performed due to the cost and time of a test. Therefore, it is necessary to find a blood-based biomarker that replaces endoscopy. The objective of the study is to identify a new inflammatory marker that replaces endoscopy by comparing blood samples of patients with inflammatory bowel disease with those of general controls.

Registry
clinicaltrials.gov
Start Date
August 1, 2016
End Date
December 30, 2020
Last Updated
6 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Bo-In Lee
Responsible Party
Sponsor Investigator
Principal Investigator

Bo-In Lee

Professor, MD, PhD.

Seoul St. Mary's Hospital

Eligibility Criteria

Inclusion Criteria

  • people who receive colonoscopy
  • people who sign the consent
  • having inflammatory bowel disease (ulcerative colitis, Crohn's Dz.) and irritable bowel syndrome

Exclusion Criteria

  • those aged over 75 years
  • the disabled
  • pregnant women
  • chronic renal diseases (CLcr \<50ml/min)
  • blood coagulopathy (PT INR \> 1.5, aPTT \> 45 seconds, or platelet count \< 50,000/mm)
  • people who refuse to sign the consent

Outcomes

Primary Outcomes

measurement of blood-based biomarkers to predict disease activity 1

Time Frame: within 12 weeks of the blood sampling

REG3 alpha (ng/mL)

measurement of blood-based biomarkers to predict disease activity 2

Time Frame: within 12 weeks of the blood sampling

hs-CRP (mg/dL)

measurement of blood-based biomarkers to predict disease activity 3

Time Frame: within 12 weeks of the blood sampling

serum calprotectin (ng/mL)

Secondary Outcomes

  • Gender (M/F)(at the time of study enrolled)
  • Age (years)(at the time of study enrolled)
  • disease onset (years)(at the time of study enrolled)
  • disease duration (months)(at the time of study enrolled)

Study Sites (1)

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