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Prednisolone in Active Ankylosing Spondylitis (AS)

Primary Purpose

Ankylosing Spondylitis

Status
Unknown status
Phase
Phase 2
Locations
Germany
Study Type
Interventional
Intervention
prednisolone
Sponsored by
Charite University, Berlin, Germany
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Ankylosing Spondylitis focused on measuring treatment, ankylosing spondylitis, prednisolone, trial, steroid

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: ankylosing spondylitis according to the modified NY criteria 1984 age between 18 and 70 years insufficient response to therapy with NSAIDs BASDAI > 4 Previous therapy with DMARDs (such as sulfasalazine, methotrexate etc.) or steroids less than or equal to 7,5mg is allowed, should be discontinued or stable 4 weeks before study start written informed consent Exclusion Criteria: Pregnancy or lactation current severe infection or during the last 3 months suspected opportunistic infection during the past 2 months (such as Herpes zoster, cytomegaly-, Pneumocystis carinii-infection), HIV-infection Malignancies severe cardial, renal, hematological, endocrinological, pulmonal, gastrointestinal (such as peptic ulcers) neurological, hepatic (viral or toxic hepatitis) concomitant disease, uncontrolled arterial hypertension remitting thrombosis, embolism Diabetes mellitus or increased blood glucose test uncontrolled glaucoma active immunization during the past 2 weeks or planned for the next 8 weeks pathologic laboratory test results: creatinine >200 µmol/l, liver enzymes > 2,5 fold, AP >2,5 fold upper normal ranges significant pathological changes during physical examination clinical trial participation during the past 30 days before screening intake of "hard drugs" (such as cocaine, heroin) therapy with more than 7,5 mg prednisolone, intraarticular steroids during the past 4 weeks before study start current application for retirement

Sites / Locations

  • Charité Campus Benjamin-Franklin RheumatolgyRecruiting
  • Immanuel Hospital RheumatologyRecruiting
  • Rheumazentrum RuhrgebietRecruiting

Outcomes

Primary Outcome Measures

50% improvement of BASDAI after 14 days of treatment

Secondary Outcome Measures

Improvement of pain on a VAS 0 - 10
Decrease of CRP/ BSG
Number of swollen/tender joints
number of enthesitic localisations
improvement of function (BASFI)
improvement of quality of life (SF12)

Full Information

First Posted
October 25, 2005
Last Updated
September 7, 2006
Sponsor
Charite University, Berlin, Germany
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1. Study Identification

Unique Protocol Identification Number
NCT00244166
Brief Title
Prednisolone in Active Ankylosing Spondylitis (AS)
Official Title
Threecenter Placebo Controlled Three Arm Trial in Patients With Active Ankylosing Spondylitis With Prednisolone
Study Type
Interventional

2. Study Status

Record Verification Date
September 2006
Overall Recruitment Status
Unknown status
Study Start Date
May 2002 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
August 2008 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Charite University, Berlin, Germany

4. Oversight

5. Study Description

Brief Summary
to investigate whether steroids are effective in ankylosing spondylitis if steroids are effective to describe how quick they work
Detailed Description
Treatment of inflammatory rheumatic conditions with glucocorticosteroids is a mainstay in therapy. In rheumatic diseases such as rheumatoid arthritis, systemic lupus erythematodes and polymyalgia rheumatica glucocorticosteroids show a prompt effect in regards of musculoskeletal symptoms. Ankylosing spondylitis (AS) is an inflammatory rheumatic disease mainly affecting the spine. However peripheral joints, entheses and the eyes can also be affected. The rheumatic symptoms of AS patients typically show good and quick response to treatment with nonsteroidal antirheumatic drugs (NSAIDs). In contrast to rheumatoid arthritis there is no proof that disease modifying antirheumatic drugs (DMARDs) work. Surprisingly there is the common opinion, mainly based on personal experiences, that glucocorticosteroids in spondylarthropathies do not work. However there are no reliable clinical studies answering this question. In the literature of the last 20 years there are only single reports about the treatment of AS with highly dosed methylprednisolone (intravenous pulse therapy). The pretended lack of effectiveness of glucocorticosteroids surprises moreover as NSAIDs are very effective as well as local intraarticular steroid injections including the sacroiliac joints. In addition with magnetic resonance imaging acute inflammatory lesions can be visualized especially as subchondral edema in bone marrow. Besides about 70% of patients with active AS show elevated inflammatory serum markers such as erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP). Moreover we could recently that a treatment of AS patients with the monoclonal antibody against TNFa (Infliximab) is highly effective. TNFa is a very important pro-inflammatory cytokine (Brandt et al 2000). For all these reasons it is very important and urgent to perform a study for the treatment of active AS with glucocorticosteroids using evaluated measuring instruments.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ankylosing Spondylitis
Keywords
treatment, ankylosing spondylitis, prednisolone, trial, steroid

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
75 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
prednisolone
Primary Outcome Measure Information:
Title
50% improvement of BASDAI after 14 days of treatment
Secondary Outcome Measure Information:
Title
Improvement of pain on a VAS 0 - 10
Title
Decrease of CRP/ BSG
Title
Number of swollen/tender joints
Title
number of enthesitic localisations
Title
improvement of function (BASFI)
Title
improvement of quality of life (SF12)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: ankylosing spondylitis according to the modified NY criteria 1984 age between 18 and 70 years insufficient response to therapy with NSAIDs BASDAI > 4 Previous therapy with DMARDs (such as sulfasalazine, methotrexate etc.) or steroids less than or equal to 7,5mg is allowed, should be discontinued or stable 4 weeks before study start written informed consent Exclusion Criteria: Pregnancy or lactation current severe infection or during the last 3 months suspected opportunistic infection during the past 2 months (such as Herpes zoster, cytomegaly-, Pneumocystis carinii-infection), HIV-infection Malignancies severe cardial, renal, hematological, endocrinological, pulmonal, gastrointestinal (such as peptic ulcers) neurological, hepatic (viral or toxic hepatitis) concomitant disease, uncontrolled arterial hypertension remitting thrombosis, embolism Diabetes mellitus or increased blood glucose test uncontrolled glaucoma active immunization during the past 2 weeks or planned for the next 8 weeks pathologic laboratory test results: creatinine >200 µmol/l, liver enzymes > 2,5 fold, AP >2,5 fold upper normal ranges significant pathological changes during physical examination clinical trial participation during the past 30 days before screening intake of "hard drugs" (such as cocaine, heroin) therapy with more than 7,5 mg prednisolone, intraarticular steroids during the past 4 weeks before study start current application for retirement
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Joachim Sieper, Prof.
Phone
0049 30 8445
Ext
4414
Email
joachim.sieper@charite.de
First Name & Middle Initial & Last Name or Official Title & Degree
Hildrun Haibel, MD
Phone
0049 30 8445
Ext
4414
Email
hildrun.haibel@charite.de
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Joachim Sieper, Prof.
Organizational Affiliation
Charité Campus Benjamin-Franklin Rheumatology
Official's Role
Principal Investigator
Facility Information:
Facility Name
Charité Campus Benjamin-Franklin Rheumatolgy
City
Berlin
ZIP/Postal Code
12200
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Joachim Sieper, Prof.
Phone
0049 30 8445
Ext
4414
Email
joachim.sieper@charite.de
First Name & Middle Initial & Last Name & Degree
Hildrun Haibel, MD
Phone
0049 30 8445
Ext
4414
Email
hildrun.haibel@charite.de
First Name & Middle Initial & Last Name & Degree
Joachim Sieper, Prof.
First Name & Middle Initial & Last Name & Degree
Hildrun Haibel, MD
First Name & Middle Initial & Last Name & Degree
Henning C Brandt, MD
First Name & Middle Initial & Last Name & Degree
In-Ho Song, MD
Facility Name
Immanuel Hospital Rheumatology
City
Berlin
ZIP/Postal Code
14109
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Andreas Krause, Prof.
Phone
0049 30 80505
Ext
293
Email
a.krause@immanuel.de
First Name & Middle Initial & Last Name & Degree
Andreas Krause, Prof.
Facility Name
Rheumazentrum Ruhrgebiet
City
Herne
ZIP/Postal Code
44652
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Juergen Braun, Prof.
Phone
0049 2325592
Ext
131
Email
j.braun@rheumazentrum-ruhrgebiet.de
First Name & Middle Initial & Last Name & Degree
Xenofon Baraliakos, MD
Phone
0049 2325592
Ext
131
Email
xenob@onlinehome.de
First Name & Middle Initial & Last Name & Degree
Juergen Braun, Prof.
First Name & Middle Initial & Last Name & Degree
Xenofon Baraliakos, MD

12. IPD Sharing Statement

Citations:
PubMed Identifier
23625982
Citation
Haibel H, Fendler C, Listing J, Callhoff J, Braun J, Sieper J. Efficacy of oral prednisolone in active ankylosing spondylitis: results of a double-blind, randomised, placebo-controlled short-term trial. Ann Rheum Dis. 2014 Jan;73(1):243-6. doi: 10.1136/annrheumdis-2012-203055. Epub 2013 Apr 26.
Results Reference
derived

Learn more about this trial

Prednisolone in Active Ankylosing Spondylitis (AS)

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