Diverticulitis: Antibiotics or Close Observation?

Last updated: October 26, 2012
Sponsor: Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Overall Status: Trial Status Unknown

Phase

4

Condition

Intra-abdominal Infections

Treatment

N/A

Clinical Study ID

NCT01111253
09/233
80-82310-97-10039
WO 08-54
ABR 29615
2009-015004-26
NL29615.018.09
  • Ages > 18
  • All Genders
  • Accepts Healthy Volunteers

Study Summary

Rationale

The prevalence of colonic diverticular disease is increasing in Western countries. Approximately 10 to 25% of patients with diverticular disease will eventually develop an episode of acute diverticulitis. Currently conservative treatment often includes antibiotic therapy. This advice lacks sound evidence and is merely based on experts' opinion. An old clinical dogma is being clarified with this randomized trial.

Objective

Primary objective is to evaluate whether or not using antibiotics reduces to time to full recovery of an attack of uncomplicated (mild) diverticulitis. Secondary objectives are to evaluate complications, quality of life, readmission rate, recurrence rate, medical and non-medical costs, and antibiotic resistance/sensitivity in both groups.

Hypothesis

The investigators hypothesis is that in the treatment of uncomplicated (mild) acute diverticulitis, supportive treatment without antibiotics is a more cost-effective approach than conservative treatment with antibiotics with respect to time-to-recovery as primary outcome.

Study design

A randomized, open label, multicenter clinical trial comparing treatment of acute uncomplicated diverticulitis with antibiotics to observation and supportive care alone.

Study population

Patients 18 years or older are eligible for inclusion if they have a diagnosis of acute uncomplicated diverticulitis as demonstrated by imaging. Only patients with stages 1a and 1b according to Hinchey's classification or "mild" diverticulitis according to the Ambrosetti criteria are included.

Intervention

Conservative strategy with antibiotics: supportive measures and at least 48 hours of intravenous antibiotics (and therefore admittance to the hospital) and subsequently switch to oral antibiotics if tolerated (total duration of 10 days).

Control

Liberal strategy without antibiotics: supportive measures only. Observation and oral intake as tolerated. Admittance only if discharge criteria are not met on presentation.

Main study parameters/endpoints

The primary endpoint is time-to-recovery with a 6-month follow-up period. Secondary endpoints are occurrence of complicated diverticulitis requiring surgery or percutaneous treatment, morbidity, health related quality of life, readmission rate, recurrence rate, medical and non-medical costs, and antibiotic resistance/sensitivity.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Only left-sided uncomplicated (mild) acute diverticulitis;

  • Clinical suspicion of acute diverticulitis. For acute diagnostic work-up: ultrasoundor CT proven diverticulitis. In the case of diverticulitis-negative ultrasound inclinically suspected patients an intravenous contrast-enhanced CT scan is mandatoryfor confirmation of diverticulitis or exclusion of other pathology. CT forHinchey/Ambrosetti classification (which is a CT-based classification system) isneeded for all patients, but can be delayed 1 day in those with ultrasound diagnosis.Staging diverticulitis is defined according the modified Hinchey/Ambrosetti staging,only stages 1a and 1b and "mild" diverticulitis (1a Confined pericolic inflammation, 1b Confined small (smaller than 5cm) pericolic abscess) are included;

  • All patients with informed consent.

Exclusion

Exclusion Criteria:

  • Previous radiological (ultrasound and/or CT) proven episode of diverticulitis;

  • Colonic cancer;

  • Inflammatory bowel disease (ulcerative colitis, Crohn's disease);

  • Hinchey stages 2, 3 and 4 or "severe" diverticulitis according to the Ambrosetticriteria, which require surgical or percutaneous treatment;

  • Disease with expected survival of less than 6 months;

  • Contraindication for the use of the study medication (e.g. patients with advancedrenal failure or allergy to antibiotics used in this study);

  • Pregnancy, breastfeeding;

  • ASA (American Society of Anaesthesiologists) classification > III;

  • Immunocompromised patients;

  • Clinical suspicion of bacteraemia (i.e. sepsis);

  • The inability of reading/understanding and filling in the questionnaires;

  • Antibiotic use in the 4 weeks before admittance.

Study Design

Total Participants: 533
Study Start date:
May 01, 2010
Estimated Completion Date:
October 31, 2014

Connect with a study center

  • Ziekenhuisgroep Twente

    Almelo,
    Netherlands

    Site Not Available

  • Flevo Hospital

    Almere,
    Netherlands

    Site Not Available

  • Meander Hospital

    Amersfoort,
    Netherlands

    Site Not Available

  • Academic Medical Center

    Amsterdam,
    Netherlands

    Site Not Available

  • BovenIJ Hospital

    Amsterdam,
    Netherlands

    Site Not Available

  • Onze Lieve Vrouwe Gasthuis

    Amsterdam,
    Netherlands

    Site Not Available

  • Sint Lucas Andreas Hospital

    Amsterdam,
    Netherlands

    Site Not Available

  • Slotervaart Hospital

    Amsterdam,
    Netherlands

    Site Not Available

  • VU Medical Center

    Amsterdam,
    Netherlands

    Site Not Available

  • Gelre Hospitals

    Apeldoorn,
    Netherlands

    Site Not Available

  • Rijnstate Hospital

    Arnhem,
    Netherlands

    Site Not Available

  • Rode Kruis Hospital

    Beverwijk,
    Netherlands

    Site Not Available

  • Reinier de Graaf Gasthuis

    Delft,
    Netherlands

    Site Not Available

  • Albert Schweitzer Hospital

    Dordrecht,
    Netherlands

    Site Not Available

  • Kennemer Hospital

    Haarlem,
    Netherlands

    Site Not Available

  • Ziekenhuisgroep Twente

    Hengelo,
    Netherlands

    Site Not Available

  • Tergooi Hospital

    Hilversum,
    Netherlands

    Site Not Available

  • Spaarne Hospitals

    Hoofddorp,
    Netherlands

    Site Not Available

  • Westfries Gasthuis

    Hoorn,
    Netherlands

    Site Not Available

  • Sint Antonius Hospital

    Nieuwegein,
    Netherlands

    Site Not Available

  • Erasmus Medical Center

    Rotterdam,
    Netherlands

    Site Not Available

  • Ikazia Hospital

    Rotterdam,
    Netherlands

    Site Not Available

  • Sint Franciscus Gasthuis

    Rotterdam,
    Netherlands

    Site Not Available

  • Máxima Hospital

    Veldhoven,
    Netherlands

    Site Not Available

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