Colesevelam for the Treatment of Bile Acid Malabsorption in Patients With Crohn's Disease (COBAM)
This study has been terminated.
(insufficient enrollment)
Sponsor:
Florian Beigel
Information provided by (Responsible Party):
Florian Beigel, Klinikum der Universitaet Muenchen, Grosshadern
ClinicalTrials.gov Identifier:
NCT01203254
First received: September 15, 2010
Last updated: April 17, 2013
Last verified: April 2013
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Purpose
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.
| Condition | Intervention | Phase |
|---|---|---|
|
Crohns Disease Bile Acid Malabsorption |
Drug: Colesevelam Drug: Placebo |
Phase 4 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Intervention Model: Parallel Assignment Masking: Double Blind (Subject, Investigator) Primary Purpose: Treatment |
| Official Title: | Colesevelam for the Treatment of Bile Acid Malabsorption in Patients With Crohn's Disease |
Resource links provided by NLM:
Further study details as provided by Klinikum der Universitaet Muenchen, Grosshadern:
Primary Outcome Measures:
- Reduction of fluid stool > 30 % [ Time Frame: 4 weeks after baseline ] [ Designated as safety issue: No ]
Secondary Outcome Measures:
- Improvement of Stool Consistency [ Time Frame: 4 weeks after baseline ] [ Designated as safety issue: No ]Proportion of patients on cholestagel compared to placebo that reaches improvement of stool consistency on the Bristol stool chart of at least one point.
- Improvement of Quality of Life. [ Time Frame: 4 weeks after baseline ] [ Designated as safety issue: No ]Proportion of patients on cholestagel compared to placebo that reaches an improvement of the Quality of Life.
- Change of median liquid or soft stool frequency/per day. [ Time Frame: 4 weeks after baseline ] [ Designated as safety issue: No ]
| Enrollment: | 34 |
| Study Start Date: | October 2010 |
| Study Completion Date: | March 2013 |
| Primary Completion Date: | March 2013 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
| Placebo Comparator: Placebo |
Drug: Placebo
Placebo tablet: 3 times daily 2 tablets
|
| Active Comparator: Cholestagel |
Drug: Colesevelam
Colesevelam 625 mg tablet; 3 times daily 2 tablets
|
Eligibility| Ages Eligible for Study: | 18 Years to 65 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion criteria:
- Signed informed consent after adequate explanation of the patient information.
- Male and female patients with CD and 18 to 65 years of age in clinical remission with a Crohns Disease Activity Index (CDAI) score of 150 or less, with symptoms of functional BAM or symptoms of BAM after small bowel resection with a frequency of at least 3 to maximal 15 liquid or soft stools per day.
Stable medical treatment of CD for a minimal period of 3 months preceding the screening visit, consisting of
- either continuous oral treatment of aminosalicylate, prednisolone (a maximum 10 mg/day), azathioprine, 6-mercaptopurine, or methotrexate
- or supporting periodic treatment* with TNF-alpha AK (Infliximab, Adalimumab, Certolizumab) (for patients on TNF-alpha, dosing with TNF-alpha should coincide with baseline visit)
- Blood serum CRP value of less or equal then 1 mg/dl (10 mg/l).
- BAM assessed with a blood test on a 7α-hydroxy-4-cholesten-3-on excretion of equal or more than 50 ng/ml
Exclusion criteria:
- Allergy or hypersensitivity to any of the components of cholestagel or placebo as identified from the medical history
- Participation at another clinical trial within a period of 4 weeks before the screening visit
- Presence of any addiction, alcohol abuse or specific disease that would not allow the patient to understand the essence and requirements and potential consequences of the participation to the clinical trial
- Signs suggestive of the patient being unable to follow the visit schedule as required (for example for professional obligations)
- Treatment with cyclosporine, or tacrolimus, 3 month or less before screening
- Oral Treatment with antibiotics 3 weeks or less before screening
- Topical treatment with steroid- or mesalazine-containing applications 3 weeks or less before screening
- Treatment with bile acid bile acid binding agent (e.g. Cholestayramine)6 weeks or less before screening
- Infectious diseases (HIV, hep B, hep C, tuberculosis, listeriosis, positive clostridium-difficile-toxin- proof in faeces)
- Current presence of intra-abdominal abscess or Fistula
- Cholestatic liver disease, bowel or biliary obstruction
- Dysphagia or swallowing disorders
- Known malignancy or history of malignancy
- Having undergone intestinal surgery within 6 months from screening
- Status after intestinal surgery with more then 100cm of resected bowel.
- Short bowel syndrome
- Planned -gastrostomy, ileostomy or colostomy.
- Pregnancy and lactation
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01203254
Locations
| Germany | |
| Hochschulambulanz Med. Klinik I - Charite- | |
| Berlin, Germany, 12200 | |
| Praxis Dr. Mroß | |
| Berlin, Germany, 10318 | |
| Hamburgisches Forschungsinstitut für CED | |
| Hamburg, Germany, 20148 | |
| Universitätsklinikum des Saarlandes -Innere Medizin- | |
| Homburg, Germany, 66424 | |
| Internistische Gemeinschaftspraxis | |
| Leipzig, Germany, 04105 | |
| CED - Zentrum der Universität München - Klinikum Grosshadern | |
| Munich, Germany, 81377 | |
Sponsors and Collaborators
Florian Beigel
Investigators
| Principal Investigator: | Florian Beigel, M.D. | Klinikum der Universität München - Grosshadern |
More Information
No publications provided
| Responsible Party: | Florian Beigel, Dr. med., Klinikum der Universitaet Muenchen, Grosshadern |
| ClinicalTrials.gov Identifier: | NCT01203254 History of Changes |
| Other Study ID Numbers: | 2009-010727-91 |
| Study First Received: | September 15, 2010 |
| Last Updated: | April 17, 2013 |
| Health Authority: | Germany: Ethics Commission Germany: Federal Institute for Drugs and Medical Devices |
Keywords provided by Klinikum der Universitaet Muenchen, Grosshadern:
|
Colesevelam IBD Bile Acid Malabsorption Crohns disease |
Additional relevant MeSH terms:
|
Crohn Disease Malabsorption Syndromes Inflammatory Bowel Diseases Gastroenteritis Gastrointestinal Diseases Digestive System Diseases Intestinal Diseases Metabolic Diseases Bile Acids and Salts |
Colesevelam Gastrointestinal Agents Therapeutic Uses Pharmacologic Actions Anticholesteremic Agents Hypolipidemic Agents Antimetabolites Molecular Mechanisms of Pharmacological Action Lipid Regulating Agents |
ClinicalTrials.gov processed this record on May 16, 2013