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OpenTrials
Completed

NCT Number: NCT00450086

Budesonide Capsules vs. Mesalazine Granules vs. Placebo in Collagenous Colitis

The purpose of this study is to determine whether budesonide or mesalazine is more active in the treatment of collagenous colitis.

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Center of digestive diseases

Hamburg, 20249, Germany

About this study

This study will check the reproducibility of the results reported in trials with budesonide in patients with collagenous colitis. Efficacy of mesalazine was never tested in collagenous colitis by placebo-controlled trials. This trial will check the superiority of mesalazine over placebo using the common clinical symptom of collagenous colitis, which is chronic or recurrent non-bloody, watery diarrhea.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

(main):

  • > 4 watery/soft stools on at least 4 days in the week prior to baseline
  • > 3 stools per day on average within the last 7 days prior to baseline
  • Symptoms (chronic watery diarrhea) for at least 3 months before baseline
  • Complete colonoscopy within the last 12 weeks before baseline
  • Histologically confirmed diagnosis of collagenous colitis

Exclusion criteria

  • Evidence of infectious diarrhea
  • Celiac disease
  • Endoscopic-histologic findings, which may have caused diarrhea
  • History of partial colonic resection
  • Diarrhea as a result of the presence of other symptomatic organic disease of the gastrointestinal tract
  • Active colorectal cancer or a history of colorectal cancer
  • Severe co-morbidity substantially reducing life expectancy
  • Abnormal hepatic function or liver cirrhosis (ALT, AST or AP >= 2 x ULN)
  • Abnormal renal function (Cystatin C > ULN)
  • Active peptic ulcer disease, local intestinal infection
  • Asthma, diabetes mellitus, infection, osteoporosis, glaucoma, cataract, or cardiovascular disease if careful medical monitoring is not ensured
  • Hemorrhagic diathesis

Treatment and study plan

Budesonide

Drug

9 mg per day

Mesalazine

Drug

3 g per day

Placebo

Drug

0 g per day

Primary outcomes

  1. Rate of clinical remission (<= 3 stools per day) after 8 weeks

    Time frame: 8 weeks

Secondary outcomes

  1. Rate of clinical remission (<= 3 stools per day) after 2 weeks

    Time frame: 2 weeks

  2. Time to remission

  3. Impact on stool consistency (watery/soft/solid)

    Time frame: 8 weeks

  4. Impact on abdominal pain

    Time frame: 8 weeks

  5. Impact on patient's general well-being

    Time frame: 8 weeks

  6. Effect on histopathology

    Time frame: 8 weeks

  7. Severity of diarrhea

    Time frame: 8 weeks

  8. QoL

    Time frame: 8 weeks

  9. PGA

    Time frame: 8 weeks

Sponsors and collaborators

Lead sponsor

Dr. Falk Pharma GmbH

Industry

Registry information

Official study title

Double-blind, Double-dummy, Randomised, Placebo-controlled, Multi-centre Phase III Clinical Study on the Efficacy and Tolerability of Budesonide Capsules vs. Mesalazine Granules vs. Placebo for Patients With Collagenous Colitis.

Important dates

Study start
2007
Primary completion
2011
Study completion
2011
First posted
Mar 21, 2007
Registry last updated
May 19, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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