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Study on Cannabinoid Receptor Expression in Gastrointestinal Diseases

M

Medical University of Graz

Status

Completed

Conditions

Colon Cancer
Ulcerative Colitis
Crohn's Disease

Study type

Observational

Funder types

Other

Identifiers

NCT02735941
KLI 521-B31

Details and patient eligibility

About

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.

Full 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.

Enrollment

31 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

31 participants in 4 patient groups

UC group
Description:
Patients with ulcerative colitis (active or remission)
CD group
Description:
Patients with Crohn's disease (active or remission)
Colon cancer group
Description:
Patients with colon cancer or metastasis
control group
Description:
healthy individuals

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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