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Dexamethasone Versus Methylprednisolone for the Treatment of Active Inflammatory Bowel Disease

Primary Purpose

Inflammatory Bowel Disease (IBD)

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Dexamethasone
Methylprednisolone
Sponsored by
University of Chicago
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Inflammatory Bowel Disease (IBD) focused on measuring Inflammatory Bowel Disease (IBD)

Eligibility Criteria

6 Years - 19 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Parental informed consent Subjects 6 to 19 years of age with confirmed diagnosis of IBD (Crohn's disease, ulcerative colitis or indeterminate colitis), who on admission to the hospital have a PCDAI>15 or a Clinical-Activity Index for the Evaluation of Patients with Ulcerative Colitis of >10. Infectious causes (viruses, bacteria, parasites) have been ruled out. Exclusion Criteria: Subjects in which the administration of corticosteroids would be contraindicated such as systemic or enteric infections diagnosed by stool analysis including culture, Clostridium Difficile toxin assay, rotavirus or adenovirus 40/41 antigens. Subjects with enterostomy or colostomy Subjects with one or more of the following conditions: unstable vital signs, acute abdomen, toxic megacolon, intestinal obstruction, intestinal perforation

Sites / Locations

  • University of Chicago Comer Children's Hospital

Outcomes

Primary Outcome Measures

Pediatric Crohn's Disease Activity Index (PCDAI)
Clinical-Activity Index for the Evaluation of Patients with Ulcerative Colitis

Secondary Outcome Measures

Partial Harvey Bradshaw score (pHB)

Full Information

First Posted
September 7, 2005
Last Updated
September 4, 2013
Sponsor
University of Chicago
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1. Study Identification

Unique Protocol Identification Number
NCT00152620
Brief Title
Dexamethasone Versus Methylprednisolone for the Treatment of Active Inflammatory Bowel Disease
Official Title
Dexamethasone Versus Methylprednisolone for the Treatment of Active Inflammatory Bowel Disease
Study Type
Interventional

2. Study Status

Record Verification Date
September 2013
Overall Recruitment Status
Terminated
Why Stopped
study completed
Study Start Date
June 2004 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
May 2007 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Chicago

4. Oversight

5. Study Description

Brief Summary
The aim of this therapeutic trial is to compare the response of subjects with active IBD to daily intravenous dexamethasone versus the response to daily intravenous methylprednisolone.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Inflammatory Bowel Disease (IBD)
Keywords
Inflammatory Bowel Disease (IBD)

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
Double
Allocation
Randomized
Enrollment
40 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Dexamethasone
Intervention Type
Drug
Intervention Name(s)
Methylprednisolone
Primary Outcome Measure Information:
Title
Pediatric Crohn's Disease Activity Index (PCDAI)
Title
Clinical-Activity Index for the Evaluation of Patients with Ulcerative Colitis
Secondary Outcome Measure Information:
Title
Partial Harvey Bradshaw score (pHB)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Years
Maximum Age & Unit of Time
19 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Parental informed consent Subjects 6 to 19 years of age with confirmed diagnosis of IBD (Crohn's disease, ulcerative colitis or indeterminate colitis), who on admission to the hospital have a PCDAI>15 or a Clinical-Activity Index for the Evaluation of Patients with Ulcerative Colitis of >10. Infectious causes (viruses, bacteria, parasites) have been ruled out. Exclusion Criteria: Subjects in which the administration of corticosteroids would be contraindicated such as systemic or enteric infections diagnosed by stool analysis including culture, Clostridium Difficile toxin assay, rotavirus or adenovirus 40/41 antigens. Subjects with enterostomy or colostomy Subjects with one or more of the following conditions: unstable vital signs, acute abdomen, toxic megacolon, intestinal obstruction, intestinal perforation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Barbara S Kirschner, MD
Organizational Affiliation
University of Chicago
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Chicago Comer Children's Hospital
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60637
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
14127503
Citation
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Citation
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Citation
Boumpas DT, Paliogianni F, Anastassiou ED, Balow JE. Glucocorticosteroid action on the immune system: molecular and cellular aspects. Clin Exp Rheumatol. 1991 Jul-Aug;9(4):413-23.
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PubMed Identifier
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Citation
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PubMed Identifier
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Citation
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Dexamethasone Versus Methylprednisolone for the Treatment of Active Inflammatory Bowel Disease

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