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

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-80
SponsorIRCCS Ospedale San Raffaele

About this trial

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.

Eligibility criteria

Qualifiers

Patients who have signed informed consent

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

Disqualifiers

Immunosuppressed patients

Patients suffering chronic inflammatory diseases

Patients with concomitant malignancy, cardiac, renal and haepatic failure

History of major vascular surgery (aneurysmectomy)

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

60 Participants
are grouped into 1 trial group

Sponsors and collaborators