Study on Cannabinoid Receptor Expression in Gastrointestinal Diseases

Sponsor
Medical University of Graz (Other)
Overall Status
Completed
CT.gov ID
NCT02735941
Collaborator
(none)
31
1
13.4
2.3

Study Details

Study Description

Brief Summary

The purpose of the study is to investigate phospholipid ligands and their receptors in inflammatory bowel diseases and colon cancer. Several new species of lipids have been recently discovered which are able to transmit information to cancer cells in the large intestine. The lipids and their responsive receptors build an axis that is thought to influence the development of inflammation and cancer.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Expression of cannabinoid receptors are examined in mucosal biopsies of the colon and blood leukocytes of patients with inflammatory bowel disease (IBD) or colon cancer in comparison to healthy individuals by polymerase chain reaction, Western Blots and flow cytometry. Colonic endoscopic biopsies and blood are collected from adult patients with confirmed active Ulcerative colitis (UC) and Crohn's disease (CD), adult UC and CD patients in remission, colon cancer patients and from healthy individuals (controls). Biopsies from healthy individuals (control group) will have undergone colonoscopy during standard screening for colorectal cancer or for the diagnostic workup of gastrointestinal symptoms without endoscopic or histologic evidence of colonic disease. For UC patients, duration and location of disease (Montreal classification), endoscopic (Mayo score) and clinical activity score, histological features and current and previous treatments (5-aminosalicylic acid, corticosteroids, immunomodulators) will be recorded. For CD patients, duration and location of disease is assessed, a HarveyBradshaw Index and activity will be scored, histological features and current and previous treatments will be recorded. Blood is collected and immediately processed for flow cytometric experiments. Phospholipids are measured in serum and in colonic mucosal biopsy samples of all cohorts by mass spectrometry.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    31 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Expression of G Protein-coupled Receptors and Ligands in Inflammatory Bowel Diseases and Colon Cancer
    Actual Study Start Date :
    Jun 13, 2017
    Actual Primary Completion Date :
    Jul 27, 2018
    Actual Study Completion Date :
    Jul 27, 2018

    Arms and Interventions

    Arm Intervention/Treatment
    UC group

    Patients with ulcerative colitis (active or remission)

    CD group

    Patients with Crohn's disease (active or remission)

    Colon cancer group

    Patients with colon cancer or metastasis

    control group

    healthy individuals

    Outcome Measures

    Primary Outcome Measures

    1. Analysis of cannabinoid receptors in blood leukocytes and biopsies from patients with IBD and colon cancer [within 24 months]

      Protein content of cannabinoid receptors and G protein-coupled receptor 55 are measured by flow cytometry in blood leukocytes of patients with ulcerative colitis or Crohn's disease, and of healthy individuals. Transcripts of cannabinoid receptors and G protein-coupled receptor 55 are also measured in colonic mucosal biopsies of IBD/colon cancer patients and healthy individuals by polymerase chain reaction.

    Secondary Outcome Measures

    1. Assessment of endoscopic activity scores (Mayo, Harvey Bradshaw index) in IBD patients. [within 24 months]

    2. Assessment of malignancy of colon cancer by tumor staging [within 24 months]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Diagnosis of Ulcerative colitis (active/remission)

    • or Crohn's disease (active/remission)

    • or Colon cancer (or metastasis)

    Exclusion Criteria:
    • unable to give informed consent

    • pregnancy

    • intermittent illness or comorbidity during Crohn/Ulcerative colitis

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Medical University of Graz Graz Austria

    Sponsors and Collaborators

    • Medical University of Graz

    Investigators

    • Principal Investigator: Rudolf Schicho, PhD, Medical University of Graz

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Medical University of Graz
    ClinicalTrials.gov Identifier:
    NCT02735941
    Other Study ID Numbers:
    • KLI 521-B31
    First Posted:
    Apr 13, 2016
    Last Update Posted:
    Jul 30, 2018
    Last Verified:
    Jul 1, 2018
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jul 30, 2018