Arthritis, Reactive Clinical Trial
Official title:
Phase 3 Trial to Assess the Efficacy of Long-term (6 Months) Combination Antibiotics as a Treatment for Chlamydia-induced Reactive Arthritis
Reactive arthritis, also known as Reiter's syndrome, is a form of arthritis that occurs as a reaction to an infection elsewhere in the body. It is characterized by inflammation of the joints, tendons, urogenital tract, and eyes. Pain and swelling in the knees, ankles, and feet are common. This study will determine the effectiveness of antibiotic therapy in treating people with chlamydia-induced reactive arthritis that has lasted for more than 6 months.
The initial infection that causes reactive arthritis is caused by one of two bacteria:
Chlamydia trachomatis, which is usually acquired through sexual contact, or Chlamydia
pneumoniae, which can cause respiratory infections. Most people recover fully from the
initial flare of arthritis symptoms. However, about 20% of people with reactive arthritis
experience long-lasting symptoms. In these individuals, the Chlamydia bacteria exist in a
persistent metabolically active state within the joint tissue, even years after the initial
exposure. The bacteria produce heat shock proteins (HSPs), which are thought to play a key
role in the chronic persistent state of Chlamydia and which may stimulate the immune
inflammatory response seen in reactive arthritis. This indicates the need for antimicrobial
therapy that can reduce Chlamydia's HSP production and block its metabolism. The purpose of
this study is to determine the effectiveness of long-term combination antibiotic therapy in
treating people with chronic reactive arthritis. The study will use two different
combinations of common antibiotics: doxycycline paired with rifampin and azithromycin paired
with rifampin.
This study will entail 6 months of treatment followed by 3 months of follow-up. After
screening, eligible participants will be randomly assigned to one of three treatment groups:
rifampin once a day plus doxycycline twice a day; rifampin once a day plus azithromycin once
a day for 5 days, then twice weekly; or placebo. Study visits will occur at baseline and
Months 1, 3, 6, and 9. At all visits, participants will undergo an interview, a physical
examination, and blood collection. They will also complete a questionnaire related to their
symptoms and functional status. At screening and Month 6, a synovial biopsy may be performed.
This will involve taking a sample of the tissue that lines the joints.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT00001679 -
Prognostic Indicators and Determinants of the 2-5 Year Outcome in a Cohort of Early Synovitis Patients
|
N/A | |
Completed |
NCT00001375 -
The Pathogenesis of Inflammatory Synovitis: A Study of Early Arthritis
|
N/A |