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Mesalazine Granules vs. Placebo for the Prevention of Recurrence of Diverticulitis

Phase 3
Terminated
Conditions
Diverticulitis
Interventions
Drug: Placebo
Registration Number
NCT00695643
Lead Sponsor
Dr. Falk Pharma GmbH
Brief Summary

The purpose of the study is to determine whether mesalazine granules compared to placebo is effective in prevention of recurrence of disease.

Detailed Description

The purpose of the study is to demonstrate the superiority of mesalazine granules compared to placebo in terms of the primary efficacy variable proportion of recurrence-free patients within 48 weeks.

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
345
Inclusion Criteria
  • Diagnosis of left-sided uncomplicated diverticular disease confirmed by ultrasonography or computed tomography
  • Presence of at least one diverticulum of the left colon
  • Most recent attack of left-sided uncomplicated diverticulitis responding to antibiotics and/or dietary modification within the last 6 months
  • C-reactive protein (CRP) > upper limit of normal (ULN) at the start of the most recent attack
Exclusion Criteria
  • Complicated diverticular disease
  • Right-sided diverticulitis
  • Previous colonic surgery
  • Presence of symptomatic organic disease of the gastrointestinal tract
  • Active colorectal cancer or a history of colorectal cancer
  • Hemorrhagic diathesis
  • Active peptic ulcer disease, local intestinal infection
  • Asthma if careful medical monitoring is not ensured
  • Abnormal hepatic function or liver cirrhosis
  • Abnormal renal function

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
BPlacebo-
AMesalazine-
Primary Outcome Measures
NameTimeMethod
Proportion of recurrence-free patients within 48 weeks48 weeks
Secondary Outcome Measures
NameTimeMethod
Health assessment48 weeks
Severity of diarrhea48 weeks
Quality of Life (QoL)48 weeks
Occurrence of diverticulitis-associated fever48 weeks
Number of days with left lower quadrant pain48 weeks
Stool consistency48 weeks
Time to recurrence
Assessment of efficacy by investigator and patient48 weeks

Trial Locations

Locations (1)

Evang. Krankenhaus Kalk, Medical department

🇩🇪

Cologne, Germany

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