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临床试验/NCT00701350
NCT00701350已完成不适用

Identification of Proteomic Markers of Intra-amniotic Infection (IAI) in Patients With Preterm Premature Rupture of Amniotic Membranes (PPROM)

ProteoGenix, Inc.4 个研究点 分布在 1 个国家目标入组 79 人开始时间: 2008年6月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
79
试验地点
4
主要终点
Expression of protein biomarkers in cervial vaginal fluid

研究概览

简要总结

The purpose of this study is to investigate the expression of protein biomarkers in cervical vaginal fluid in women with preterm premature rupture of membranes (PPROM)

详细描述

Preterm premature rupture of the membranes (PPROM) prior to 37 weeks of gestation occurs in approximately 3% of all pregnancies and is associated with one-third of all preterm births (Mercer, 2003). While there are multiple possible etiologies of PPROM, intra-amniotic infection has been implicated as a major contributor, especially at early gestational ages where fetal and neonatal adverse sequelae are frequent (Yoon, et al. 2000). Micro-organisms are recovered from the amniotic fluid obtained by trans-abdominal amniocentesis in 25-40% of women at the time of presentation with PPROM (Simhan and Canavan 2005).

Significant risks to the fetus following PPROM include both complications related to prematurity and to infection or inflammation (ACOG Practice Bulletin 2007). Complications related to prematurity include respiratory distress, intraventricular hemorrhage, and necrotizing enterocolitis. IAI, both clinically apparent and occult, is an important and potentially preventable cause of cerebral white matter injury and cerebral palsy. Ideally, an early diagnosis of IAI in the setting of PPROM is important to allow timely treatment and intervention. Amniocentesis is successful from 40 - 72% of the time with PPROM (Garite, 1982, Blackwell and Berry, 1999). Despite the accuracy for determining infection and the feasibility of amniocentesis, the vast majority of clinicians are reluctant and/or unwilling to perform this procedure in this clinical setting (Capeless and Mead, (1987). There is therefore a critical need for a noninvasive test to identify patients with IAI and PPROM. Timely identification of these sub-clinically infected patients is critical in designing rationale and efficacious treatment strategies that may reduce the fetal and neonatal sequelae associated with PPROM.

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
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Subject is 18 years of age or older
  • Subject has singleton gestation
  • Subject has fetus with getstational age of at least 23 0/7 days and no greater than 33 6/7 days
  • Subject has diagnosis of preterm premature rupture of amniotic membranes as determined by at least two of the following:
  • Postive pooling,
  • Presence of ferning from cervical vaginal fluid swab on an air dried slide,
  • Postivie nitrizine pH test, or, in lieu of the criteria listed above
  • Positive Amnisure test result
  • Positive indigo carmine egress vaginally following instillation at amniocentesis
  • Subject is enrolled and has an amniocentesis within 24 hours of membrane rupture
  • Subject is a candidate for expectant management as evidenced by the following:
  • Absence of labor (defined by absence of painful uterine contractions)
  • No clinical signs of infection (maternal fever of 37.9 C or greater, fetal heart rate greater than 160 bpm, uterine tenderness, purulent aminorrhea)
  • presence of non-reassuring heart tracing
  • Subject is a candidate for amniocentesis as evidenced by the following:
  • Ultrasound reveals pocket of fluid likely to result in successful amniocentesis
  • Physician believes that the subject shoudl undergo amniocentesis as part of their routine evaluation of their current problem of PPROM to rule out infection and/or to test for lung maturity

排除标准

  • Subject has a fetus with major fetal anomaly (life threatening or requires surgical intervention) or chromosomal aneuploidy
  • Subject has pre-existing medical indication for preterm delivery (e.g., pre-eclampsia, refractory hypertension, diabetes with significant complications, active lupus)
  • Subject is unable to provide informed consent

结局指标

主要结局

Expression of protein biomarkers in cervial vaginal fluid

时间窗: 24 hours of amniotic membrane rupture to delivery

次要结局

未报告次要终点

研究者

发起方
ProteoGenix, Inc.
申办方类型
Industry

研究点 (4)

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