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Completed

NCT Number: NCT02445365

Remote Ischemic Conditioning in Patients With Ulcerative Colitis

Ulcerative colitis (UC) is a chronic relapsing inflammatory bowel disease (IBD). At the time of diagnosis it is not possible to predict the course of the disease, which can range from a few flares in a lifetime to uncontrollable disease leading to hospitalization, surgery and stoma. There is a continuous need to improve treatment as well as diagnostic and prognostic tools.

This study evaluates the clinical efficacy, tolerability and feasibility of remote ischemic conditioning (RIC) in patients with moderate active ulcerative colitis (UC). The investigators hypothesize that RIC beyond the well known effect on reperfusion tissue damage has a clinically relevant anti-inflammatory effect in UC. RIC constitute a repeated brief and non-harmful suppression of blood circulation in a limb. The mechanism of action of RIC is likely to involve suppressed inflammation and cell death.

Our study is a randomized clinical controlled study including 38 patients. Patients will receive RIC or sham for 10 consecutive days.

The effect of RIC on active UC is evaluated by changes patient's symptoms, endoscopy findings, and various markers in the blood, faeces and the intestinal wall.

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Key information

Age range

18 year–99 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Odense University Hospital

Odense, 5000, Denmark

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age:≥18 years
  • Verified ulcerative colitis diagnosis according to clinical, endoscopic and histological standard criteria.
  • Diagnosis of ulcerative colitis established for at least 6 months
  • Moderate active ulcerative colitis, total Mayo score > 6
  • Endoscopic subscore activity grade ≥1
  • Written informed consent

Exclusion criteria

  • Pancolitis or acute severe ulcerative colitis requiring immediate treatment
  • Need for admission due to active ulcerative colitis
  • Ulcerative colitis with systemic symptoms (abdominal pain, fever > 37.5 degrees, weight loss exceeding 3 kilograms).
  • Patient with anemia (Haemoglobin < 8.3 mmol/l for males and < 7.3 mmol/l for females).
  • Patient with ostomy or pouch.
  • The patient has had a bowel resection (except appendectomy)
  • The patient has constipation and/or another known bowel condition than ulcerative colitis such as IBS.
  • The patient has diabetes.
  • Regular intake of acetylsalicylic acid or NSAIDs
  • The patient cannot understand the information material.
  • The patient has had colon cancer, dysplasia or adenomatous polyps in the colon during the recent 5 year
  • The patient is in a poor general condition.
  • The patient has had a food poisoning within the last three months.
  • The patient is pregnant at the time of inclusion or has planned pregnancy during the period of study.
  • The patient is in medical treatment with cyclosporine at the beginning of the run in period.
  • Treatment for ulcerative colitis treatment has been changed within two weeks before the first day in the run in period
  • The patient has commenced treatment with azathioprine, 6-mercaptopurine or methotrexate within 12 weeks before the first day in the run in period.
  • The patient has commenced treatment with TNF-α inhibitors within 12 weeks before the first day of the run in period.
  • The patient suffers from coeliac disease or lactose intolerance.
  • Antibiotic treatment within two weeks before the first day of the run in period.
  • Patient has any medical, surgical condition that excludes the use of RIC.

Treatment and study plan

AutoRIC device

Device

Primary outcomes

  1. Change in index of clinical activity - numerical change in Mayo score including endoscopic subscore

    Time frame: 10 days

Secondary outcomes

  1. Change in fecal calprotectin.

    Time frame: 10 days

  2. Change in endoscopy - central reading according to Mayo endoscopic subscore and UCEIS

    Time frame: 10 days

  3. Number of patients achieving clinical remission (Mayo score <3)

    Time frame: 10 days

  4. Patient experience of repeated RIC (questionnaire, including placebo recognition).

    Time frame: 10 days

  5. Change in histological score of inflammation.

    Time frame: 10 days

  6. Changes in serum and mucosal cytokine profile in particular Th1/Th2/Th9/Th17/Th22. measured by FlowCytomix Multiplex.

    Time frame: 10 days

  7. Changes in serum markers of inflammation (serum C-reactive protein).

    Time frame: 10 days

  8. Changes in serum markers of extracellular matrix proteins (C1M, C3M, C4M, P1NP and VICM).

    Time frame: 10 days

  9. Changes in serum and mucosal level of CGRP, endothelin-1, endothelin-2.

    Time frame: 10 days

  10. Effect of RIC in patients with active ulcerative colitis using the Langendorff model (to document activation of a cardioprotective response).

    Time frame: 10 days

Sponsors and collaborators

Lead sponsor

Odense University Hospital

Other

Collaborators

  • Aarhus University Hospital
  • University of Southern Denmark

Registry information

Official study title

Effect of Remote Ischemic Conditioning (RIC) on Inflammation and Remodelling of Extracellular Matrix Proteins in Patients With Inflammatory Bowel Diseases

Important dates

Study start
2015
Primary completion
2018
Study completion
2018
First posted
May 15, 2015
Registry last updated
Mar 22, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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