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Adverse Effects of Glucocorticoid Therapy on Bone in Childhood Crohn's Disease

Primary Purpose

Crohn Disease

Status
Unknown status
Phase
Phase 4
Locations
United Kingdom
Study Type
Interventional
Intervention
prednisolone
Alicalm (polymeric liquid formula)
Sponsored by
University Hospital Birmingham
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Crohn Disease focused on measuring Crohn Disease, Children, Bone Density, Prednisolone, Liquid Diet Therapy, Quality of Life, Metabolic Bone Disease

Eligibility Criteria

7 Years - 17 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Active Crohn's Disease with PCDAI > 20
  • Aged 7 - 17 with possibility of 1 year follow-up

Exclusion Criteria:

  • Previous treatment for Crohn's Disease with liquid diet or glucocorticoid therapy
  • Isolated orofacial granulomatosis
  • Intravenous glucocorticoid therapy immediately indicated
  • Planned surgical intervention for CD

Sites / Locations

  • Royal Liverpool Children's HospitalRecruiting
  • Oxford Children's HospitalRecruiting
  • Sheffield Children's HospitalRecruiting
  • Birmingham Children's HospitalRecruiting
  • Bristol Royal Hospital for Sick ChildrenRecruiting
  • St George's University HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

1

2

Arm Description

Outcomes

Primary Outcome Measures

Bone mineral density change based on DXA measurement at 1 year

Secondary Outcome Measures

Proportion in remission
Change in PCDAI, HAB and pHBS
Quality of life throughout treatment period, using IMPACT III measurements
Baseline urine 11B-HSD1 and bone formation
Baseline urine 11B-HSD1 activity and change in bone mineral density
Change in urine 11B-HSD1 activity and PCDAI in patients before and after treatment with LDT and CST
Growth impairment
Adherence to randomised therapy for relapses
Adverse effects

Full Information

First Posted
January 24, 2008
Last Updated
December 29, 2008
Sponsor
University Hospital Birmingham
Collaborators
SHS International, Children's Memorial Research Foundation, St George's University Hospital Research Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT00609752
Brief Title
Adverse Effects of Glucocorticoid Therapy on Bone in Childhood Crohn's Disease
Official Title
Adverse Effects of Glucocorticoid Therapy on Bone in Childhood Crohn's Disease
Study Type
Interventional

2. Study Status

Record Verification Date
December 2008
Overall Recruitment Status
Unknown status
Study Start Date
February 2008 (undefined)
Primary Completion Date
January 2010 (Anticipated)
Study Completion Date
January 2010 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
University Hospital Birmingham
Collaborators
SHS International, Children's Memorial Research Foundation, St George's University Hospital Research Foundation

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study will compare two current first-line treatments for childhood Crohn's Disease, steroids versus a liquid diet, and determine the effects of these treatments on bone health, quality of life and treatment efficacy.
Detailed Description
Crohn's Disease is a very serious inflammatory gut disorder that often first presents in childhood. Once present, the underlying condition remains for life. It usually responds well to medical treatment which brings about a disease 'remission' but is inclined to become active again at intervals (relapses). When it is active, children are very unwell with reduced energy, loss of appetite and distressing abdominal symptoms (pain, diarrhea, etc.). Active disease can be treated in two very different ways - either with a 3-month course of steroids (tablets), or with a 6-week course of so called "liquid diet therapy (LDT)." With LDT, children receive all of their nutrition in liquid form. Both treatments have advantages and disadvantages. Both are quite effective, often controlling symptoms within days. Steroids may cause various side effects including thinning of bones (osteoporosis) with increased risk of fractures. LDT is somewhat challenging because normal (solid) foods are not allowed during the period of treatment. Both steroids and LDT are widely used - steroids predominately in the USA and LDT elsewhere. There is controversy as to which is best. This study aims to determine which should be preferred. In this clinical study, children presenting with Crohn's disease will be randomly assigned to either steroid treatment or LDT and followed up for a period of one year. During that time the assigned treatment will be used for any episodes of active disease. We will study a total of 80 children attending the Paediatric Gastroenterology Units in Birmingham, Bristol, Liverpool, Oxford, Sheffield and St. George's Hospital in London. Various outcomes will be compared in the two groups. We will examine the recovery rates (success in bringing about remission) and the frequency of subsequent relapses. We will compare growth and physical development, because active Crohn's disease and possibly steroids may have adverse effects on these processes. A special focus of the study will be on the effect of the disease and its treatment on bone health. Using special blood and urine tests and bone scans we will compare bone growth and density in the two groups. Finally, it is crucially important that we consider the impact of the disease and its treatment on the young person on the basis of their own individual perspective. To do this we will compare the 'quality of life' of children in the two treatment groups, using a questionnaire specially designed to measure this aspect in young people with Crohn's disease. This study will thus enable us to undertake a comprehensive comparison of the two major first-line treatments used in childhood Crohn's Disease. This is crucially important, and no such study has previously been undertaken

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Crohn Disease
Keywords
Crohn Disease, Children, Bone Density, Prednisolone, Liquid Diet Therapy, Quality of Life, Metabolic Bone Disease

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
80 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Active Comparator
Arm Title
2
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
prednisolone
Intervention Description
Standard treatment regimens based on body weight will be used (approximately 2 mg per kg), with a stepwise dose reduction over a 10-14 week period.
Intervention Type
Dietary Supplement
Intervention Name(s)
Alicalm (polymeric liquid formula)
Other Intervention Name(s)
Alicalm (SHS International Ltd.)
Intervention Description
Subjects will receive all of their nutritional requirements in the form of a nutritionally balanced polymeric feed, volume based on EAR for age. Duration of 5 to 8 weeks with subjects returning to a "normal" unrestricted diet by 10 weeks.
Primary Outcome Measure Information:
Title
Bone mineral density change based on DXA measurement at 1 year
Time Frame
12 months post-recruitment
Secondary Outcome Measure Information:
Title
Proportion in remission
Time Frame
6 weeks
Title
Change in PCDAI, HAB and pHBS
Time Frame
6 weeks
Title
Quality of life throughout treatment period, using IMPACT III measurements
Time Frame
12 months
Title
Baseline urine 11B-HSD1 and bone formation
Time Frame
6 weeks
Title
Baseline urine 11B-HSD1 activity and change in bone mineral density
Time Frame
12 months
Title
Change in urine 11B-HSD1 activity and PCDAI in patients before and after treatment with LDT and CST
Time Frame
12 months
Title
Growth impairment
Time Frame
12 months
Title
Adherence to randomised therapy for relapses
Time Frame
12 months
Title
Adverse effects
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
7 Years
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Active Crohn's Disease with PCDAI > 20 Aged 7 - 17 with possibility of 1 year follow-up Exclusion Criteria: Previous treatment for Crohn's Disease with liquid diet or glucocorticoid therapy Isolated orofacial granulomatosis Intravenous glucocorticoid therapy immediately indicated Planned surgical intervention for CD
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
M. Stephen Murphy
Phone
+44 (0)121 333 8705
Email
m.s.murphy@bham.ac.uk
First Name & Middle Initial & Last Name or Official Title & Degree
Kelly Spencer
Phone
+44 (0)121 333 9542
Email
k.spencer@bham.ac.uk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
M. Stephen Murphy
Organizational Affiliation
University of Birmingham
Official's Role
Study Director
Facility Information:
Facility Name
Royal Liverpool Children's Hospital
City
Liverpool
State/Province
Merseyside
ZIP/Postal Code
L12 2AP
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mark Dalzell
Facility Name
Oxford Children's Hospital
City
Oxford
State/Province
Oxfordshire
ZIP/Postal Code
OX3 9DZ
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Astor Rodrigues
Facility Name
Sheffield Children's Hospital
City
Sheffield
State/Province
South Yorkshire
ZIP/Postal Code
S10 2TH
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Christopher Taylor
Facility Name
Birmingham Children's Hospital
City
Birmingham
State/Province
West Midlands
ZIP/Postal Code
B4 6NH
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kelly Spencer
Phone
+44 (0)121 333 9542
Email
k.spencer@bham.ac.uk
First Name & Middle Initial & Last Name & Degree
M Stephen Murphy
Facility Name
Bristol Royal Hospital for Sick Children
City
Bristol
ZIP/Postal Code
BS2 8BJ
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Christine Spray
Facility Name
St George's University Hospital
City
London
ZIP/Postal Code
SW17 0QT
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sally Mitton

12. IPD Sharing Statement

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Adverse Effects of Glucocorticoid Therapy on Bone in Childhood Crohn's Disease

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