Crohn's Disease and Colitis Trial, By Invitation NCT07662902 Sponsor: University Hospital Dubrava Condition: Crohn's Disease and Colitis
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Crohn's Disease and Colitis Trial, By Invitation

NCT07662902
By Invitation Not Applicable

voxsanity.com.au · Eligibility summary from public government registries · 18 August 2026 · not medical advice

Who may and may not be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who may be able to join

  • Adults between 18 and 70 years of age.
  • People who have been diagnosed with ulcerative colitis (a type of inflammatory bowel disease) for at least 6 months, based on recognised European guidelines.
  • People whose ulcerative colitis is currently in clinical remission, meaning their symptom score is very low (partial Mayo score below 2).
  • People whose ulcerative colitis is in biochemical remission, meaning a stool test shows low levels of inflammation (fecal calprotectin below 100 μg/g).
  • People who are able to have a FibroScan, which is a non-invasive scan used to assess the liver, and for whom that scan produces reliable results.
  • People who are willing and able to provide written consent to take part before the study begins.

Who may not be able to join

Each point below is a reason the trial team may not be able to accept someone. It is not a list of requirements to meet.

  • People whose ulcerative colitis affects only the rectum (the very last part of the bowel), based on their most recent scope examination.
  • People who drink alcohol above certain weekly limits — more than 140 grams per week for women, or more than 210 grams per week for men (confirm with trial site for what this means in standard drinks).
  • People whose FibroScan produces results that are not considered reliable.
  • People who have a known long-term liver condition from another cause, including autoimmune, viral, alcohol-related, metabolic, or cancerous liver disease.
  • People who have advanced liver disease where the liver is no longer able to function properly (decompensated cirrhosis).
  • People who test positive for hepatitis B or hepatitis C.
  • People who have coeliac disease (an immune reaction to gluten).
  • People who have type 1 diabetes.
  • People who have a history of cancer.
  • People whose liver enzyme levels (ALT or AST) are more than five times higher than the normal range.
  • People whose liver is affected by congestion due to heart failure.
  • People who have a blockage in the bile ducts causing abnormal liver enzyme results.
  • People who have cancer that has spread to the liver.
  • People who have a blood clot in the portal vein (the main vein supplying the liver).
  • People who have Budd-Chiari syndrome, a condition affecting blood flow out of the liver.
  • People who are pregnant.
  • People who are unable or unwilling to provide written consent to participate.

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 14 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

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Trial details

Status
By Invitation
Phase
Not Applicable
Sponsor
University Hospital Dubrava
Registry
ClinicalTrials.gov
Start date
1 December 2025
Est. completion
1 January 2027

Where this trial is recruiting

🇭🇷 Croatia

Primary endpoints

Correlation Between Serum Zonulin Concentration and Liver Stiffness Measurement (LSM); Correlation Between Serum Lipopolysaccharide-Binding Protein (LBP) Concentration and Liver Stiffness Measurement (LSM)

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 14 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov