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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04535882
Other study ID # LRG
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date October 1, 2020
Est. completion date December 31, 2024

Study information

Verified date June 2023
Source Showa Inan General Hospital
Contact Akira Horiuchi, MD
Phone 81265822121
Email horiuchi.akira@sihp.jp
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

We attempt to examine the association between serum leucine-rich alpha-2 glycoprotein (LRG) levels and endoscopic activity in patients with possible ulcerative colitis (UC) or Crohn's disease (CD) to determine whether LRG was a predicting marker for UC or CD.


Description:

Serum samples were collected from patients, and scores for clinical and endoscopic activity of disease were obtained by reviewing the clinical records of patients. Serum sampling and colonoscopy with histology were performed within 7 days.The disease activity of UC and CD patients was evaluated by the Mayo score and Crohn disease activity index (CDAI), respectively. The Mayo endoscopy score was evaluated. UC patients whose Mayo endoscopy score was 2 or 3 were divided into the active UC group. CD patients whose CDAI >150 were divided into the active CD group.


Recruitment information / eligibility

Status Recruiting
Enrollment 125
Est. completion date December 31, 2024
Est. primary completion date December 31, 2024
Accepts healthy volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Patients whom possible UC or Crohn disease was suspected Exclusion Criteria: - other autoimmune diseases - acute or chronic renal failure - chronic heart diseases - liver cirrhosis - cancer - acute or chronic infections - ischemic colitis - infectious colitis

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
serum leucine-rich alpha-2 glycoprotein (LRG) levels
Patients who were diagnosed with possible UC or Crohn disease according to endoscopic, radiological, histological, and clinical criteria were enrolled. Serum samples were collected from patients, and scores for clinical and endoscopic activity of disease were obtained by reviewing the clinical records of patients. Serum sampling and colonoscopy were performed within 7 days.

Locations

Country Name City State
Japan Showa Inan General Hospital Komagane Nagano

Sponsors (1)

Lead Sponsor Collaborator
Showa Inan General Hospital

Country where clinical trial is conducted

Japan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Serum LRG measurement Serum samples were collected from patients, and scores for clinical and endoscopic activity of disease were obtained by reviewing the clinical records of patients. one year