ClinicalTrials.gg
Not yet recruitingNCT07027007DIVENDOUpdated Jun 18, 2025

Prospective Observational Analysis of Circulating Endocan Levels in Patients Presenting With Acute Diverticulitis

An observational study in Diverticulitis, sponsored by IRCCS Ospedale San Raffaele. Not yet recruiting at 1 site in Italy. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2025-06-18.

Sponsored by IRCCS Ospedale San Raffaele · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
60
Ages
18 Years to 80 Years
Sex
All
01

Study summary

Quantify the level of endocan in blood samples collected from patients with acute diverticulitis in the emergency department. Determine if endocan levels are correlated with the severity of diverticulitis according to the WSES classification. Assess whether patients requiring emergency surgical intervention have higher endocan values compared to others.

02

Conditions studied

  • Diverticulitis

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Keywords

  • endocan
  • acute diverticolitis
  • diverticulitis classification
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 60 is below the median of 275 across 59 observational studies indexed under Diverticulitis.

Browse Diverticulitis studies →

Lead sponsor

IRCCS Ospedale San Raffaele is the lead sponsor of 36 studies on the registry; 28 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Patients affected by acute diverticulitis in the emergency department

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

  • Patients who have signed
  • Patients who are affected by acute diverticulitis after clinical evaluation and imaging (i.e. u.s. or CeCT)

Exclusion criteria

Exclusion Criteria:

  • patients
  • Patients suffering chronic inflammatory diseases
  • Patients with concomitant , cardiac, renal and haepatic failure
  • History of major vascular surgery (aneurysmectomy)
  • Pregnant women
  • Patients participating in other studies that may interfere with the outcome of the intervention.
Terms in these criteria, in plain language(3)

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

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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.

Immunosuppression

A weakened immune system. It can come from an illness, such as HIV or some blood cancers, or from medicines that turn the immune system down, for example after an organ transplant or for an autoimmune disease; steroids at higher doses count.

Read whether the line is about a condition or about medicines, and which medicines and doses it means.

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
60 participants (estimated)
Target follow-up
12 Months
Patient registry
Yes
Biospecimen retention
Samples without dna

Groups and cohorts

  • patients with acute diverticulitis

    Patients admitted to the emergency department with acute diverticulitis classified according to WSES statements.

06

What researchers measure

Primary outcomes

  1. Endocan serum level at admission

    To evaluate the correlation between blood concentration of endocan and severity of diverticulitis

    Time frame: The serum of the patients enrolled inthe study will be collected within two hours from emergency room registation and tested for ENDOCAN

Secondary outcomes

  1. Predictive value of endocan in determining which patients need emergency surgery

    Concentration of endocan in grade 3-4 WSES compared to grade1-2

    Time frame: Patients will undergo diverticulitis evaluations (per WSES criteria) within 3 hours of Emergency room admission and study enrollment

  2. Prognostic value of endocan in determining the risk of recurrent diveritculitis

    Concentration of endocan in patient who develop a recurrence after 1 year follow-up

    Time frame: From discharge after definitive tretament till 12 months follow-up

07

Study locations

1 site
  • Emergency Department IRCCS San Raffaele
    Milano, 20132, Italy
    • Luca Ghirardelli, MD · Contactghirardelli.luca@hsr.it · +393282342663
    • Luca Ghirardelli, MD · Principal investigator
08

References and documents

Individual participant data

Plan to share: Yes — All IPD that underlie results in a publication

Supporting information: Study protocol, Statistical analysis plan, Informed consent form, Clinical study report, Analytic code

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 18, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07027007
Lead sponsor
IRCCS Ospedale San Raffaele
Responsible party
Luca Ghirardelli (MD, IRCCS Ospedale San Raffaele) — Principal investigator
First posted
Jun 18, 2025
Start date
Sep 30, 2025 (estimated)
Primary completion
Sep 2026 (estimated)
Completion
Sep 2027 (estimated)
Last update
Jun 18, 2025

Oversight

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 Jun 2025. You cannot join it, but the record below documents what was studied.

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