Mesalazine Granules vs. Placebo for the Prevention of Recurrence of Diverticulitis
- 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
Group Intervention Description B Placebo - A Mesalazine -
- Primary Outcome Measures
Name Time Method Proportion of recurrence-free patients within 48 weeks 48 weeks
- Secondary Outcome Measures
Name Time Method Health assessment 48 weeks Severity of diarrhea 48 weeks Quality of Life (QoL) 48 weeks Occurrence of diverticulitis-associated fever 48 weeks Number of days with left lower quadrant pain 48 weeks Stool consistency 48 weeks Time to recurrence Assessment of efficacy by investigator and patient 48 weeks
Trial Locations
- Locations (1)
Evang. Krankenhaus Kalk, Medical department
🇩🇪Cologne, Germany