ClinicalTrials.gg
Active, not recruitingNCT06023004Updated Feb 6, 2026

The Diverticulitis Study

An observational study in Colonic Diverticulitis, Colorectal Cancer and Acute Diverticulitis, sponsored by University of Aarhus. Active, not recruiting at 5 sites in Denmark. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-02-06.

Sponsored by University of Aarhus · Observational

Study type
Observational
Model
Case-control
Time perspective
Prospective
Enrollment
250
Ages
18 Years and older
Sex
All
01

Study summary

Acute colonic diverticulitis is when a part of the colon gets swollen and inflamed. The diagnosis is based on a CT scan, which can show thickening of the colonic walls and infiltration of the diverticula. These changes and the concomitant symptoms can overlap with colorectal cancer (CRC). Therefore, the guidelines suggest that people with diverticulitis should be offered a colonoscopy to ensure, that CRC is not the underlying cause of the changes and symptoms.

In Denmark, a lot of people get hospitalized each year due to diverticulitis, and many of them end up having colonoscopies with the purpose of excluding CRC. Currently, there are no methods for guiding colonoscopies following a diverticulitis episode, resulting in numerous unnecessary colonoscopies each year.

In the Diverticulitis study, we want to investigate if a simple blood test analyzed for the presence of circulating tumor DNA (ctDNA), can help us decide who needs a colonoscopy. We will collect blood samples from 220 people with diverticulitis and categorize them into ctDNA positive and negative groups. The ctDNA category will be compared to the colonoscopy results to see if there is a correlation between being ctDNA positive and having a CRC diagnosed at the colonoscopy.

This study could change clinical practice since we anticipate that ctDNA-guided triaging of diverticulitis patients is a cost-effective strategy for selecting diverticulitis patients needing colonoscopy, ensuring detection of the underlying CRC, and significantly reducing the number of patients undergoing unnecessary colonoscopy.

Read the detailed description

KEY POINTS

  • Colonoscopy is recommended after acute diverticulitis to rule out CRC, and yearly more than 2000 colonoscopies are performed.
  • CRC incidence is low in the diverticulitis population and most colonoscopies are unnecessary. It takes approximately 100-200 colonoscopies to diagnose just 1 CRC.
  • ctDNA is a minimally invasive and extraordinarily powerful biomarker of cancer.

GOALS

● To use ctDNA analysis to triage diverticulitis patients for colonoscopy. Diagnosing the same CRCs, but minimizing the number of patients needing colonoscopy

PERSPECTIVES

  • Practice-changing evidence for ctDNA-guided triaging of diverticulitis patients for colonoscopy, an important and well-recognized clinical dilemma in the management of CRC.
  • Evaluation of the cost-effectiveness of ctDNA-guided triaging versus standard-of-care.

PROJECT DESCRIPTION For patients who have experienced an episode of acute colonic diverticulitis, Danish and international guidelines recommend opportunistic screening with colonoscopy to rule out CRC as the underlying reason for the diverticulitis symptoms. In Denmark, there are more than 4000 hospitalizations per year due to diverticulitis. Accordingly, a substantial number of post-diverticulitis colonoscopies are performed each year to rule out underlying CRC. Colonoscopy is an invasive procedure associated with discomfort and pain in more than 50% of patients. The procedure also carries the risk of complications such as perforation and hemorrhage, particularly for patients with diseased intestines such as diverticulitis patients. CRC prevalence in suspected diverticulitis patients is low, \<2% overall, and as low as 0.5% for uncomplicated diverticulitis. Thus, an unreasonably high number of colonoscopies, ranging from 50 and up to more than 200, are needed to diagnose 1 CRC. In comparison, a >4% CRC prevalence is considered the minimal acceptable among patients selected for follow-up colonoscopy in the Danish nationwide CRC screening program, corresponding to less than 25 colonoscopies per CRC. Hence, it may be questioned whether the current guidelines on follow-up colonoscopy after diverticulitis are at all acceptable, both from a patient perspective and from a health-economy perspective. However, it has been very difficult to change. Consequently, there is an urgent need for a highly sensitive, low-risk, minimally invasive cancer detection test that can be used to triage newly diagnosed diverticulitis patients and ensure that underlying CRC is still diagnosed while minimizing the number of patients needing colonoscopy. Here, we propose to conduct a case/control study to explore the feasibility of using our recently developed TriMeth ctDNA analysis test for this purpose.

We hypothesize that ctDNA analysis can triage diverticulitis patients for colonoscopy and achieve a diagnosis of prevalent CRC but at a substantially lower colonoscopy/CRC ratio. For this purpose, we will use our tumor-agnostic ctDNA analysis "TriMeth". TriMeth was originally developed as a CRC screening tool for selecting individuals from the average-risk population for colonoscopy. Accordingly, the threshold for calling the test positive was set with the objective of high specificity. At 99% specificity, it has a sensitivity of 85%. Based on data from the original development and validation cohorts (400 CRC and 800 controls), we will tailor TriMeth for this specific purpose, i.e., setting the threshold for test positivity to achieve near 100% sensitivity by accepting a lower specificity. Second, we will conduct a case-control study to validate this new TriMeth-diverticulitis threshold in the target population. We expect a minimum of 20 cases with CRC diagnosed at colonoscopy after suspected diverticulitis to be identified through the IMPROVE study (NCT03637686). For each case, 10 controls will be randomly selected (to a minimum of 200 total) from patients with CT-verified diverticulitis and a follow-up colonoscopy without CRC. Diverticulitis patients may at the time of colonoscopy exhibit symptoms, that would in any case serve as an absolute indication for colonoscopy (patients age >40 with changes in bowel habits >1 month, rectal bleeding, iron-deficiency anemia, or excessive weight-loss). Therefore, in addition to blood sampling, we will at the time of CRC diagnosis or negative colonoscopy collect information on other established indicators for colonoscopy. As part of the study, we will conduct a health-economy assessment comparing the TriMeth-guided approach to the current practice of "colonoscopy for all". The primary outcome is the sensitivity and specificity of TriMeth for CRC detection in this population. The secondary outcome is health economy, considering the other indicators for colonoscopy. If high sensitivity and clinically and economically relevant colonoscopy-sparing potential is demonstrated, the data will be presented to the Danish Colorectal Cancer Group and the Danish Health Technology Council with the aim of obtaining approval to change the national guideline and implement the approach.

02

Conditions studied

  • Colonic Diverticulitis
  • Colorectal Cancer
  • Acute Diverticulitis
03

In context

Diverticulitis, Colonic

27 studies on the registry are indexed under Diverticulitis, Colonic; 8 are open to participants now.

This study's planned enrollment of 250 is close to the median of 250 across 15 observational studies indexed under Diverticulitis, Colonic.

Browse Diverticulitis, Colonic studies →

Lead sponsor

University of Aarhus is the lead sponsor of 1,300 studies on the registry; 189 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients with newly CT-verified diverticulitis will be identified by the attending physician at the recruiting surgical departments. Patients fulfilling the inclusion criteria are approached and invited to participate.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • CT-verified diverticulitis eligible for a follow-up colonoscopy

Exclusion criteria

Exclusion Criteria:

  • Unable to provide oral and written
  • Recent colonic imaging and no need for renewed visualization of the colonic mucosa deemed by the attending doctor
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Observational model
Case-control
Time perspective
Prospective
Enrollment
250 participants (estimated)
Patient registry
No
Biospecimen retention
Samples with dna

Groups and cohorts

  • Controls

    Patients diagnosed with diverticulitis through CT scan and scheduled for a colonoscopy. The colonoscopy must result in no detection of colorectal cancer.

  • Cases

    Patients diagnosed with CRC immediately after an episode of diverticulitis.

06

What researchers measure

Primary outcomes

  1. ctDNA analysis

    Blood samples will be categorized as either ctDNA positive or negative

    Time frame: After recruitment of the last patient, we expect that ctDNA analyses can be performed within 6 months

Secondary outcomes

  1. Cost-effectiveness of treatment

    Assessment of the cost-effectiveness of "ctDNA guided" versus "opportunistic" colonoscopy screening of the diverticulitis patients

    Time frame: After recruitment of the last patient, we expect that cost-effectiveness analyses can be performed within 12 months

07

Study locations

5 sites
08

References and documents

Publications

  • Andersen JC, Bundgaard L, Elbrond H, Laurberg S, Walker LR, Stovring J; Danish Surgical Society. Danish national guidelines for treatment of diverticular disease. Dan Med J. 2012 May;59(5):C4453. PubMed 22549495 ↗
  • Meyer J, Orci LA, Combescure C, Balaphas A, Morel P, Buchs NC, Ris F. Risk of Colorectal Cancer in Patients With Acute Diverticulitis: A Systematic Review and Meta-analysis of Observational Studies. Clin Gastroenterol Hepatol. 2019 Jul;17(8):1448-1456.e17. doi: 10.1016/j.cgh.2018.07.031. Epub 2018 Jul 26. PubMed 30056181 ↗
  • Jensen SO, Ogaard N, Orntoft MW, Rasmussen MH, Bramsen JB, Kristensen H, Mouritzen P, Madsen MR, Madsen AH, Sunesen KG, Iversen LH, Laurberg S, Christensen IJ, Nielsen HJ, Andersen CL. Novel DNA methylation biomarkers show high sensitivity and specificity for blood-based detection of colorectal cancer-a clinical biomarker discovery and validation study. Clin Epigenetics. 2019 Nov 14;11(1):158. doi: 10.1186/s13148-019-0757-3. PubMed 31727158 ↗
  • Jensen SO, Ogaard N, Nielsen HJ, Bramsen JB, Andersen CL. Enhanced Performance of DNA Methylation Markers by Simultaneous Measurement of Sense and Antisense DNA Strands after Cytosine Conversion. Clin Chem. 2020 Jul 1;66(7):925-933. doi: 10.1093/clinchem/hvaa100. PubMed 32460325 ↗
  • Ogaard N, Reinert T, Henriksen TV, Frydendahl A, Aagaard E, Orntoft MW, Larsen MO, Knudsen AR, Mortensen FV, Andersen CL. Tumour-agnostic circulating tumour DNA analysis for improved recurrence surveillance after resection of colorectal liver metastases: A prospective cohort study. Eur J Cancer. 2022 Mar;163:163-176. doi: 10.1016/j.ejca.2021.12.026. Epub 2022 Jan 22. PubMed 35074652 ↗
09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 6, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06023004
Responsible party
Sponsor
First posted
Sep 5, 2023
Start date
May 1, 2022
Primary completion
May 1, 2024
Completion
May 2030 (estimated)
Last update
Feb 6, 2026

Study contacts

Thomas Bjørsum-Meyer, MD, PhD
principal investigator · Odense University Hospital
Per V Andersen, MD, PhD
principal investigator · Odense University Hospital
Kåre A Gotschalck, MD, PhD
principal investigator · Regionshospitalet Horsens
Liza Sopina, PhD
principal investigator · University of Southern Denmark

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Feb 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion