The purpose of this study is to assess the efficacy of cholestagel to reduce the frequency of soft and liquid stools per day in patients with CD in clinical remission with symptoms of BAM and to assess the improvement in stool consistency and quality of life in these patients and to assess the safety of cholestagel.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
34
Colesevelam 625 mg tablet; 3 times daily 2 tablets
Placebo tablet: 3 times daily 2 tablets
Praxis Dr. Mroß
Berlin, Germany
Hochschulambulanz Med. Klinik I - Charite-
Berlin, Germany
Hamburgisches Forschungsinstitut für CED
Hamburg, Germany
Universitätsklinikum des Saarlandes -Innere Medizin-
Homburg, Germany
Reduction of fluid stool > 30 %
Time frame: 4 weeks after baseline
Improvement of Stool Consistency
Proportion of patients on cholestagel compared to placebo that reaches improvement of stool consistency on the Bristol stool chart of at least one point.
Time frame: 4 weeks after baseline
Improvement of Quality of Life.
Proportion of patients on cholestagel compared to placebo that reaches an improvement of the Quality of Life.
Time frame: 4 weeks after baseline
Change of median liquid or soft stool frequency/per day.
Time frame: 4 weeks after baseline
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Internistische Gemeinschaftspraxis
Leipzig, Germany
CED - Zentrum der Universität München - Klinikum Grosshadern
Munich, Germany