New Immunomodulatory Therapy Strategies in Chronic Reactive Arthritis

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT00244179
Recruitment Status : Unknown
Verified September 2006 by Charite University, Berlin, Germany.
Recruitment status was:  Recruiting
First Posted : October 26, 2005
Last Update Posted : September 8, 2006
Information provided by:
Charite University, Berlin, Germany

Brief Summary:
  1. to investigate, whether one of the two alternative therapy strategies (antibiotic plus immunostimulation versus antibiotic plus immunosuppression) in chronic reactive arthritis is therapeutical superior to conventionel standardtherapy (DMARD).
  2. to investigate, whether one or more of the different therapy strategies cause an altered detection of bacterial DNA in the joint or colon.
  3. to measure the antigen-specific and -unspecific immune response (predominantly t-cell response) during therapy and correlate it with the clinical course.
  4. to gain knowledge from these analyses and the clinical course concerning the pathogenesis and the point of attack for possible therapies in chronic reactive arthritis.
  5. to compare cytokine-profiles of CD4- and CD8-positive T-cells from patients treated with infliximab to those treated with etanercept.

Condition or disease Intervention/treatment Phase
Reactive Arthritis Drug: interferon-gamma Drug: infliximab Drug: dmard Phase 2

  Show Detailed Description

Study Type : Interventional  (Clinical Trial)
Enrollment : 40 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Educational/Counseling/Training
Official Title: New Immunomodulatory Therapy Strategies in Chronic Reactive Arthritis: Immunostimulation Plus Antibiotic Versus Immunosuppression Plus Antibiotic Versus Conventional Standardtherapy
Study Start Date : January 2003

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Arthritis

Primary Outcome Measures :
  1. change in intensity of pain (VAS pain, scale 0-10)
  2. change in funcion (WOMAC)

Secondary Outcome Measures :
  1. decrease of CRP/ESR
  2. change of cytokine response
  3. change of DNA detection
  4. number of swollen and tender joints
  5. number of entheseal localisations
  6. improvement of quality of life, „Short form 36“ (SF-36)
  7. BASDAI (disease activity index)
  8. Reduction of NSAIDs
  9. Patient`s global (scale 0-10).
  10. Physician`s global (scale 0-10).

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 70 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  1. definite classification of the arthritis as ReA enteric ReA is defined as an arthritis, which occurs within 4 weeks after a preceding symptomatic infection of the gut with enteric bacteria such as yersinia, salmonella, campylobacter jejuni, shigella. If no symptomatic preceding infection can be remembered the triggering enterobacterium has to be clearly identified by serology or stool culture. Other causes for a diarrhea like for example inflammatory bowel disease have to be eliminated.

    urogenital (chlamydia-triggered) ReA is defined as an arthritis, which occurs within 4 weeks after a symptomatic urogenital infection or an infection of the upper airways or if chlamydia can be clearly identified be serology or direct proof.

  2. disease duration > 12 months
  3. age 18 to 70 years
  4. active arthritis in at least one joint
  5. constant demand of NSAIDs
  6. intensity of pain > 4 on a visual analogue scale (VAS; 0 to 10)
  7. patients are allowed to have been treated with so-called conventional therapy (Sulphasalazine, Methotrexate etc.) or steroids i.a. before, but they have to be stopped 4 weeks before enrolled into the trial
  8. able to self-administer s.c. injections or have a caregiver who will do so
  9. women of child bearing potential must have a negative pregnancy test at study baseline and use an adequate, effective method of contraception (such as implants, injectables, combined oral contraceptives, some IUDs, sexual abstinence, vasectomised partner) for a duration of 6 months after stop of therapy. Sexual active men must use an accepted method of contraception for a duration of 6 months after stop of therapy.
  10. reading a normal chest/ lung x-ray, negative Mendel-Mantoux-skin test (10,0 TE) (both not older than 4 weeks). If Mendel-Mantoux-skin test is positive and / or there are hints for a healed up tuberculosis in the chest x-ray (latent tuberculosis) and the patient shall receive infliximab or etanercept an additional therapy with isoniazid 300 mg daily starting 4 weeks before first administration of infliximab or etanercept has to be given.
  11. signed informed consent

Exclusion Criteria:

  1. female subjects who are pregnant or breast-feeding
  2. previous treatment with cytokines or anti-cytokines (biological agents)
  3. severe infections within the last 3 months
  4. history of opportunistic infections within the last 2 months (herpes zoster, cytomegaly virus-, pneumocystis carinii-infection)
  5. HIV-infection
  6. history of malignancy
  7. receipt of any live (attenuated) vaccines within last 30 days before screening visit
  8. previous diagnosis or signs of demyelinating diseases
  9. history of uncontrolled diabetes, unstable ischemic heart disease, active inflammatory bowel disease, active peptic ulcer disease, recent stroke, ongoing congestive heart failure, and any other condition which, in the opinion of the investigator, would put the subject at risk by participation in the protocol.
  10. history of cytopenia
  11. laboratory exclusions are: hemoglobin level < 8,5 g/dl, white blood cell count < 3.5 x109/l, platelet count < 125 x 109 /l, creatinine level > 175 µmol/ liver enzymes > 1,5, alkaline phosphatase >2 times the upper limit of normal, Quick > 50.
  12. clinical examination showing significant abnormalities of clinical relevance
  13. participation in trials of other investigational medications within 30 days of entering the study
  14. history or current evidence of abuse of ”hard” drugs (e.g. cocaine/heroine)
  15. current medication with 7,5 mg or more Prednisolon daily

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT00244179

Contact: joachim sieper, prof. 0049 30 8445 ext 4414
Contact: henning c brandt, md 0049 30 8445 ext 4414

Charite Campus Benjamin Franklin, Rheumatology Recruiting
Berlin, Germany, 12200
Contact: joachim sieper, prof.    0049 30 8445 ext 4414   
Contact: henning c brandt, md    0049 30 8445 ext 4414   
Principal Investigator: joachim sieper, prof         
Sub-Investigator: henning c brandt, md         
Sub-Investigator: hildrun haibel, md         
Sub-Investigator: in-ho song, md         
Sub-Investigator: Martin Rudwaleit, MD         
Sponsors and Collaborators
Charite University, Berlin, Germany
Principal Investigator: joachim sieper, prof. charite, campus benjamin franklin, rheumatology, berlin Identifier: NCT00244179     History of Changes
Other Study ID Numbers: ReA01
First Posted: October 26, 2005    Key Record Dates
Last Update Posted: September 8, 2006
Last Verified: September 2006

Keywords provided by Charite University, Berlin, Germany:
reactive arthritis

Additional relevant MeSH terms:
Arthritis, Reactive
Joint Diseases
Musculoskeletal Diseases
Arthritis, Infectious
Spinal Diseases
Bone Diseases
Antineoplastic Agents
Antiviral Agents
Anti-Infective Agents
Dermatologic Agents
Gastrointestinal Agents
Antirheumatic Agents