ClinicalTrials.gg
Not yet recruitingNCT07824180AUDUpdated Sep 21, 2026

Improving the Treatment of Acute Uncomplicated Diverticulitis in Routine Care

An interventional study of standardized treatment algorithm in Diverticulitis, sponsored by Ente Ospedaliero Cantonale, Bellinzona. Not yet recruiting. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-09-21.

Sponsored by Ente Ospedaliero Cantonale, Bellinzona · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
800
Allocation
Non-randomized
Ages
18 Years and older
Sex
All
01

Study summary

Acute uncomplicated diverticulitis is often treated with antibiotics, although current evidence shows that antibiotics are not always necessary. This study will evaluate whether a more standardized approach to treatment can reduce unnecessary antibiotic use without increasing the risk of treatment failure.

The study will compare patients treated before and after the new treatment approach is introduced in participating Swiss hospitals. Information on treatment, hospital admissions, complications and recurrence of diverticulitis will be collected. Patients will be followed for up to 24 months.

02

Conditions studied

  • Diverticulitis

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03

In context

Diverticulitis

125 studies on the registry are indexed under Diverticulitis; 22 are open to participants now.

This study's planned enrollment of 800 is above the median of 120 across 63 interventional studies indexed under Diverticulitis.

Browse Diverticulitis studies →

Lead sponsor

Ente Ospedaliero Cantonale, Bellinzona is the lead sponsor of 38 studies on the registry; 17 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

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

  • Age 18 years or older
  • CT-confirmirmed acute uncomplicated diverticulitis of the left colon
  • Ability to provide for participants in the prospective phase

Exclusion criteria

Exclusion Criteria:

  • Complicated acute diverticulitis, defined as diverticulitis with abscess, perforation (free air), fistula, or distant free fluid
  • Diverticulitis of the right or transverse colon

    -.Alternative diagnosis explaining the participant's symptoms

  • No possibility of completing the 90-day follow-up
  • Inability to provide for the prospective phase
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

Phase
Not applicable
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
800 participants (estimated)

Study arms

  • Other
    Antibiotic Treatment

    Participants with acute uncomplicated diverticulitis who receive antibiotic treatment according to the standardized treatment approach.

    Other: standardized treatment algorithm

  • Other
    No Antibiotic Treatment Arm Description:

    Participants with acute uncomplicated diverticulitis who are managed without antibiotics according to the standardized treatment approach.

    Other: standardized treatment algorithm

Interventions

  • Otherstandardized treatment algorithm

    A standardized treatment approach based on clinical findings, laboratory results, comorbidities, immunosuppression status, and CT findings is introduced to support treatment decisions in patients with acute uncomplicated diverticulitis. Depending on these factors, patients may be managed with or without antibiotics.

06

What researchers measure

Primary outcomes

  1. Treatment failure

    Treatment failure is defined as a composite outcome including progression to complicated diverticulitis requiring percutaneous abscess drainage or surgery, delayed initiation of antibiotics after initial management without antibiotics, or unplanned hospital admission following initial outpatient treatment.

    Time frame: Within 90 days after diagnosis

Secondary outcomes

  1. Antibiotic use

    Proportion of participants receiving antibiotics

    Time frame: Within 90 days after diagnosis

  2. Adherence to the standardized treatment approach

    Proportion of participants whose management is consistent with the standardized treatment approach.

    Time frame: At the initial treatment decision

  3. Outpatient versus inpatient management

    Proportion of participants initially managed as outpatients versus inpatients.

    Time frame: At the initial treatment decision

  4. Hospital admission

    Proportion of participants readmitted to hospital.

    Time frame: Within 30 days after diagnosis

  5. Recurrence of diverticulitis

    Proportion of participants experiencing recurrence of diverticulitis.

    Time frame: Within 24 months after diagnosis

07

Study locations

No study locations are listed for this record.

08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for Oct 2026; primary completion for Apr 2027, 6 months later.

Of 16 interventional studies with no phase under Diverticulitis, half reached primary completion within 36 months of starting (the median), counting those still running; a quarter within 12 and three quarters within 57. This study's planned 6 months is below that.

How these figures are worked out, and which studies are left out of them.

Registered
Sep 11, 2026
First posted
Sep 17, 2026
StartEst.
Oct 2026
Primary completionEst.
Apr 2027
CompletionEst.
Jul 2027
Last update
Sep 21, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Sep 21, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07824180
Lead sponsor
Ente Ospedaliero Cantonale, Bellinzona
Responsible party
Sponsor
First posted
Sep 17, 2026
Start date
Oct 2026 (estimated)
Primary completion
Apr 2027 (estimated)
Completion
Jul 2027 (estimated)
Last update
Sep 21, 2026

Study contacts

Dimitri Christoforidis, MD
Contact
Dimitrios.Christoforidis@eoc.ch
Elena Porro, Msc
Contact
ricerca.chirurgiaorl@eoc.ch
0041918117038
Dimitri Christoforidis, MD
principal investigator · EOC

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 not yet recruiting, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.

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