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临床试验/NCT00351273
NCT00351273已完成3 期

Phase 3 Trial to Assess the Efficacy of Long-term (6 Months) Combination Antibiotics as a Treatment for Chlamydia-induced Reactive Arthritis

University of South Florida3 个研究点 分布在 2 个国家目标入组 42 人开始时间: 2006年5月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
42
试验地点
3
主要终点
Investigate Whether a 6 Month Course of Combined Antibiotics Was Effective Treatment.

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Meet the following European Spondyloarthropathy Study Group Criteria:
  • inflammatory spinal pain OR
  • synovitis AND
  • one or more of the following:
  • positive family history
  • urethritis or cervicitis within 1 month prior to onset of arthritis
  • buttock pain
  • enthesopathy
  • sacroiliitis
  • Disease duration of at least 6 months
  • Negative pregnancy test at study baseline and willing to use an effective method of contraception other than combined oral contraceptives for the duration of the study (for women of childbearing age)

排除标准

  • Sensitivity or history of allergic reaction to rifampin, doxycycline, or azithromycin
  • Currently taking any medications that may interact with the study medications, specifically rifampin
  • Liver transaminases greater than or equal to two times the normal level
  • Significant abnormalities in the complete blood count (CBC)
  • Current psoriasis
  • Diagnosis of inflammatory bowel disease
  • Diagnosis of ankylosing spondylitis
  • Previous prolonged exposure to antibiotics (more than 2 weeks) as a potential treatment for reactive arthritis

研究组 & 干预措施

Azithromycin and Rifampin

Active Comparator

Participants received Azithromycin and Rifampin

干预措施: Azithromycin and Rifampin (Drug)

Doxycycline and Rifampin

Active Comparator

Participants received Doxycycline and Rifampin

干预措施: Doxycycline and Rifampin (Drug)

received placebo

Placebo Comparator

Participants received placebo

干预措施: Placebo (Drug)

结局指标

主要结局

Investigate Whether a 6 Month Course of Combined Antibiotics Was Effective Treatment.

时间窗: Month 6

The outcome measure was a composite endpoint. Participants had to meet 4/6 clinical criteria. 17/24 subjects randomized to combination antibiotics did respond to treatment when compared to 3/10 randomized to placebo.

次要结局

  • PhGA Assessment(Baseline, month 1,3,6 and 9)
  • Erythrocyte Sedimentation Rate (ESR)(Baseline Month 1, 3, 6 and 9)
  • Number of Patients With a Complete Response (Resolution of All Symptoms)(Months 6 and 9)
  • Swollen 76 Joint Count (SJC)(Baseline, month 1,3,6 and 9)
  • hsCRP(Baseline, Month 1, 3, and 6)
  • HAQ DI Score(Baseline, Month 1,3,6 and 9)
  • 78 Tender Joint Count (TJC)(Baseline, Month 1, 3, 6 and 9)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (3)

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