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Observational Study of Disease Severity in Participants Diagnosed With Crohn's Disease and Long Term Impact of Treatment Strategies in Participants With Moderate to Severe Crohn's Disease (Protocol P06484)
This study is currently recruiting participants.
Verified April 2012 by Schering-Plough

First Received on October 7, 2010.   Last Updated on April 20, 2012   History of Changes
Sponsor: Schering-Plough
Information provided by (Responsible Party): Schering-Plough
ClinicalTrials.gov Identifier: NCT01218360
  Purpose

This is an observational study to determine the prevalence of moderate to severe Crohn's disease (CD) among patients with active CD and to evaluate existing therapeutic trends in a standard clinical practice.


Condition Intervention
Crohn Disease
Drug: Physician standard-of-care

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Observational Study on Disease Severity, Evaluation Tools and the Long Term Impact of Each Treatment Strategy in the Daily Clinical Practice in Patients With Moderate to Severe Active Crohn's Disease (Protocol P06484)

Resource links provided by NLM:


Further study details as provided by Schering-Plough:

Primary Outcome Measures:
  • Percentage of Crohn's disease participants among the study population with a Crohn's Disease Activity Index (CDAI) score of 220-450 at the enrollment to the study. [ Time Frame: Week 0 ] [ Designated as safety issue: No ]
  • Record of treatment strategy followed [ Time Frame: Week 0 to 2 years ] [ Designated as safety issue: No ]
  • Change in the CDAI score during the observational period [ Time Frame: Week 0 to 2 years ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Number of surgeries and hospitalizations during the observational period [ Time Frame: Week 0 to 2 years ] [ Designated as safety issue: No ]

Estimated Enrollment: 100
Study Start Date: October 2011
Estimated Study Completion Date: November 2014
Estimated Primary Completion Date: April 2012 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
Participants
All participants enrolled
Drug: Physician standard-of-care
Participants will be treated according to their physician's routine practice and the respective Summary of Product Characteristics (SmPC).

  Eligibility

Ages Eligible for Study:   18 Years to 65 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

Participants with diagnosed active Crohn's Disease who are inadequately controlled with their current therapy

Criteria

Inclusion Criteria

  1. Must have a diagnosis of active Crohn's Disease irrespective of severity,
  2. Must be inadequately controlled with their current therapy and for whom physician decides to switch treatment.
  3. Must be between 18 and 65 years of age, of either sex,
  4. Must demonstrate willingness to participate in the study by signing the written informed consent.

Exclusion Criteria

  • No specific exclusion criteria will be applied to a participant as long as the participant is eligible for the trial
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01218360

Contacts
Contact: Toll Free Number 1-888-577-8839

Locations
Greece
Vianex, S.A. / MSD Recruiting
Alimos, Greece, GR-174-55
Contact: Platon Peristaris     302109897322        
Sponsors and Collaborators
Schering-Plough
  More Information

No publications provided

Responsible Party: Schering-Plough
ClinicalTrials.gov Identifier: NCT01218360     History of Changes
Other Study ID Numbers: P06484
Study First Received: October 7, 2010
Last Updated: April 20, 2012
Health Authority: Greece : National Organization of Medicine EOF, Department of Clinical Trials

Keywords provided by Schering-Plough:
Crohn's disease
standard-of-care
Crohn Disease
Active Crohn's Disease

Additional relevant MeSH terms:
Crohn Disease
Inflammatory Bowel Diseases
Gastroenteritis
Gastrointestinal Diseases
Digestive System Diseases
Intestinal Diseases

ClinicalTrials.gov processed this record on May 24, 2012