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临床试验/NCT01150747
NCT01150747已完成不适用

Chlamydia Trachomatis Immunology and Vaccinology Study: Determination of Protective T Cell Responses to Chlamydia Trachomatis Infection

Harold Wiesenfeld4 个研究点 分布在 1 个国家目标入组 347 人开始时间: 2011年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
347
试验地点
4
主要终点
Determination of the chlamydia-specific cellular responses that correlates with protection against incident infection

研究概览

简要总结

The primary objective is to prospectively follow 200 women with or at risk of cervicitis to determine the chlamydia-specific cellular responses that correlate with protection against incident infection. The hypothesis is that a positive IFN-y response by peripheral CD4+ T cells responding to stimulation with HSP60 will be significantly associated with protection from incident C. trachomatis infection.

详细描述

A total of 200 women with or at high risk of having cervicitis will be prospectively followed for correlations between chlamydia-specific cellular responses and protection against incident infection.

At enrollment participants will undergo a history and physical examination; blood draw; and pelvic examination including collection of vaginal and cervical samples, STD testing and endometrial biopsy.

Participants will have follow up visits conducted at 1, 4, 8 and 12 months following enrollment. At the follow-up visits, participants will undergo a repeat history and physical, blood draw and pelvic examination including collection of vaginal and cervical samples and STD testing.

The study design will allow comprehensive identification of the antigen-specific cell mediated immune responses most strongly associated with protection against C. trachomatis infection.

The primary objective is to prospectively follow 200 women with or at risk for cervicitis to determine the chlamydia-specific cellular responses that correlate with protection against incident infection.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

入排标准

年龄范围
15 Years 至 35 Years(Child, Adult)
性别
Female
接受健康志愿者

入选标准

  • 未提供

排除标准

  • Pregnant or nursing a baby. Note: a urine pregnancy test will be done at enrollment. Result must be negative to participate in the study.
  • Gynecologic surgery or surgical abortion in preceding 2 months of enrollment.
  • Allergy to any of the study medications and/or derivatives (cephalosporins, azithromycin, erythromycin, any macrolide or ketolide antibiotic) or Type 1 hypersensitivity allergic reaction to penicillin.
  • Systemic or vaginal antibiotic therapy in preceding 7 days of enrollment.
  • Prior hysterectomy.
  • Any condition, in the opinion of the investigator that would interfere with the participant's safety or with study outcomes.
  • Participation in any study involving an investigational product in the past 30 days or anticipation of participation in any study using an investigational product in the next 30 days.
  • Previous participation in this study.

研究组 & 干预措施

Risk of positive chlamydia

  1. current, untreated endocervical C. trachomatis infection
  2. mucopurulent cervicitis on pelvic examination
  3. Sexual contact with a male partner recently diagnosed with C. trachomatis, and/or non-gonococcal urethritis

干预措施: ceftriaxone (Drug)

Risk of positive chlamydia

  1. current, untreated endocervical C. trachomatis infection
  2. mucopurulent cervicitis on pelvic examination
  3. Sexual contact with a male partner recently diagnosed with C. trachomatis, and/or non-gonococcal urethritis

干预措施: Azithromycin (Drug)

结局指标

主要结局

Determination of the chlamydia-specific cellular responses that correlates with protection against incident infection

时间窗: one year per patient

次要结局

  • Identify immunologic correlates associated with containment of the organism to the lower genital tract(one year per patient)
  • Compare chlamydia-specific cellular responses in the PBMCs to endometrial lymphocytes(one year per patient)
  • Evaluate the endocervical T cell phenotypes of women with containment of the organism to the lower genital tract(one year per patient)
  • Characterize transcriptional inflammatory responses of women with Chlamydia(Study participation one year per patient)
  • Use SNP analysis to identify genetic risk factors for chlamydia infection and disease(Study participation is one year per patient)

研究者

发起方
Harold Wiesenfeld
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Harold Wiesenfeld

Associate Professor

University of Pittsburgh

研究点 (4)

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