search
Back to results

Colesevelam for the Treatment of Bile Acid Malabsorption in Patients With Crohn's Disease (COBAM)

Primary Purpose

Crohns Disease, Bile Acid Malabsorption

Status
Terminated
Phase
Phase 4
Locations
Germany
Study Type
Interventional
Intervention
Colesevelam
Placebo
Sponsored by
Florian Beigel
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Crohns Disease focused on measuring Colesevelam, IBD, Bile Acid Malabsorption, Crohns disease

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Praxis Dr. Mroß
  • Hochschulambulanz Med. Klinik I - Charite-
  • Hamburgisches Forschungsinstitut für CED
  • Universitätsklinikum des Saarlandes -Innere Medizin-
  • Internistische Gemeinschaftspraxis
  • CED - Zentrum der Universität München - Klinikum Grosshadern

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Active Comparator

Arm Label

Placebo

Cholestagel

Arm Description

Outcomes

Primary Outcome Measures

Reduction of fluid stool > 30 %

Secondary Outcome Measures

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.
Improvement of Quality of Life.
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.

Full Information

First Posted
September 15, 2010
Last Updated
April 17, 2013
Sponsor
Florian Beigel
search

1. Study Identification

Unique Protocol Identification Number
NCT01203254
Brief Title
Colesevelam for the Treatment of Bile Acid Malabsorption in Patients With Crohn's Disease
Acronym
COBAM
Official Title
Colesevelam for the Treatment of Bile Acid Malabsorption in Patients With Crohn's Disease
Study Type
Interventional

2. Study Status

Record Verification Date
April 2013
Overall Recruitment Status
Terminated
Why Stopped
insufficient enrollment
Study Start Date
October 2010 (undefined)
Primary Completion Date
March 2013 (Actual)
Study Completion Date
March 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Florian Beigel

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Crohns Disease, Bile Acid Malabsorption
Keywords
Colesevelam, IBD, Bile Acid Malabsorption, Crohns disease

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
34 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Title
Cholestagel
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
Colesevelam
Intervention Description
Colesevelam 625 mg tablet; 3 times daily 2 tablets
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo tablet: 3 times daily 2 tablets
Primary Outcome Measure Information:
Title
Reduction of fluid stool > 30 %
Time Frame
4 weeks after baseline
Secondary Outcome Measure Information:
Title
Improvement of Stool Consistency
Description
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
Title
Improvement of Quality of Life.
Description
Proportion of patients on cholestagel compared to placebo that reaches an improvement of the Quality of Life.
Time Frame
4 weeks after baseline
Title
Change of median liquid or soft stool frequency/per day.
Time Frame
4 weeks after baseline

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility 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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Florian Beigel, M.D.
Organizational Affiliation
Klinikum der Universität München - Grosshadern
Official's Role
Principal Investigator
Facility Information:
Facility Name
Praxis Dr. Mroß
City
Berlin
ZIP/Postal Code
10318
Country
Germany
Facility Name
Hochschulambulanz Med. Klinik I - Charite-
City
Berlin
ZIP/Postal Code
12200
Country
Germany
Facility Name
Hamburgisches Forschungsinstitut für CED
City
Hamburg
ZIP/Postal Code
20148
Country
Germany
Facility Name
Universitätsklinikum des Saarlandes -Innere Medizin-
City
Homburg
ZIP/Postal Code
66424
Country
Germany
Facility Name
Internistische Gemeinschaftspraxis
City
Leipzig
ZIP/Postal Code
04105
Country
Germany
Facility Name
CED - Zentrum der Universität München - Klinikum Grosshadern
City
Munich
ZIP/Postal Code
81377
Country
Germany

12. IPD Sharing Statement

Citations:
PubMed Identifier
24953836
Citation
Beigel F, Teich N, Howaldt S, Lammert F, Maul J, Breiteneicher S, Rust C, Goke B, Brand S, Ochsenkuhn T. Colesevelam for the treatment of bile acid malabsorption-associated diarrhea in patients with Crohn's disease: a randomized, double-blind, placebo-controlled study. J Crohns Colitis. 2014 Nov;8(11):1471-9. doi: 10.1016/j.crohns.2014.05.009. Epub 2014 Jun 19.
Results Reference
derived

Learn more about this trial

Colesevelam for the Treatment of Bile Acid Malabsorption in Patients With Crohn's Disease

We'll reach out to this number within 24 hrs