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临床试验/NCT06082453
NCT06082453招募中不适用

Modernizing Perinatal Syphilis Testing

The University of Texas Health Science Center, Houston18 个研究点 分布在 1 个国家目标入组 924 人开始时间: 2023年5月2日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
924
试验地点
18
主要终点
Positive predictive value of quantitative polymerase chain reaction (qPCR) assay for detecting T. pallidum

研究概览

简要总结

The purpose of this study is to determine the testing performance of real-time quantitative polymerase chain reaction and transcription mediated amplification by comparing test performance of these novel molecular tests to current 2021 CDC CS guidelines for maternal/neonatal dyads at risk for syphilis infection and to determine whether CS is associated with adverse neurodevelopmental outcomes.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
— 至 45 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Maternal diagnosis of syphilis by 2021 CDC STI guidelines, irrespective of treatment status; AND viable pregnancy with gestational age ≥ 12 weeks OR postpartum ≤ 96 hours from delivery OR Neonates of pregnancies affected by syphilis ≤ 72 hours of birth
  • Individuals (men and non-pregnant) with syphilis in Harris Health clinic with syphilis

排除标准

  • Pregnant individuals and neonates who do not meet the criteria of syphilis (false positive)
  • Planning to move outside of study prior to ND testing

结局指标

主要结局

Positive predictive value of quantitative polymerase chain reaction (qPCR) assay for detecting T. pallidum

时间窗: from the time of birth up to 72 hours after birth

Samples will be collected from participants during the following time periods: from the time of birth to up to 72 hours after birth (for neonates) from time of birth up to 96 hours after birth (for mothers)

Sensitivity of quantitative polymerase chain reaction (qPCR) assay for detecting T. pallidum

时间窗: from the time of birth up to 96 hours after birth

Samples will be collected from participants during the following time periods: from the time of birth to up to 72 hours after birth (for neonates) from time of birth up to 96 hours after birth (for mothers)

Specificity of quantitative polymerase chain reaction (qPCR) assay for detecting T. pallidum

时间窗: from the time of birth up to 72 hours after birth

Samples will be collected from participants during the following time periods: from the time of birth to up to 72 hours after birth (for neonates) from time of birth up to 96 hours after birth (for mothers)

Negative predictive value of quantitative polymerase chain reaction (qPCR) assay for detecting T. pallidum

时间窗: from the time of birth up to 72 hours after birth

Samples will be collected from participants during the following time periods: from the time of birth to up to 72 hours after birth (for neonates) from time of birth up to 96 hours after birth (for mothers)

Area under the receiver operating characteristic (ROC) curve of quantitative polymerase chain reaction (qPCR) assay for detecting T. pallidum

时间窗: from the time of birth up to 72 hours after birth

Samples will be collected from participants during the following time periods: from the time of birth to up to 72 hours after birth (for neonates) from time of birth up to 96 hours after birth (for mothers)

Sensitivity of Aptima Treponema pallidum transcription-mediated amplification (TMA) assay for detecting T. pallidum

时间窗: from the time of birth up to 72 hours after birth

Samples will be collected from participants during the following time periods: from the time of birth to up to 72 hours after birth (for neonates) from time of birth up to 96 hours after birth (for mothers)

Specificity of Aptima Treponema pallidum transcription-mediated amplification (TMA) assay for detecting T. pallidum

时间窗: from the time of birth up to 72 hours after birth

Samples will be collected from participants during the following time periods: from the time of birth to up to 72 hours after birth (for neonates) from time of birth up to 96 hours after birth (for mothers)

Positive predictive value of Aptima Treponema pallidum transcription-mediated amplification (TMA) assay for detecting T. pallidum

时间窗: from the time of birth up to 72 hours after birth

Samples will be collected from participants during the following time periods: from the time of birth to up to 72 hours after birth (for neonates) from time of birth up to 96 hours after birth (for mothers)

Area under the receiver operating characteristic (ROC) curve of CDC 2021 STI Treatment Guidelines for diagnosis of syphilis

时间窗: from 12 weeks gestational age up to 18 months after birth

Clinical data used to diagnose syphilis according the CDC 2021 STI Guidelines will be collected as part of standard clinical care from the time of pregnancy (greater than or equal to 12 weeks gestational age) up to 18 months after birth.

Negative predictive value of Aptima Treponema pallidum transcription-mediated amplification (TMA) assay for detecting T. pallidum

时间窗: from the time of birth up to 72 hours after birth

Samples will be collected from participants during the following time periods: from the time of birth to up to 72 hours after birth (for neonates) from time of birth up to 96 hours after birth (for mothers)

Specificity of CDC 2021 STI Treatment Guidelines for diagnosis of syphilis

时间窗: from 12 weeks gestational age up to 18 months after birth

Clinical data used to diagnose syphilis according the CDC 2021 STI Guidelines will be collected as part of standard clinical care from the time of pregnancy (greater than or equal to 12 weeks gestational age) up to 18 months after birth.

Area under the receiver operating characteristic (ROC) curve of Aptima Treponema pallidum transcription-mediated amplification (TMA) assay for detecting T. pallidum

时间窗: from the time of birth up to 72 hours after birth

Samples will be collected from participants during the following time periods: from the time of birth to up to 72 hours after birth (for neonates) from time of birth up to 96 hours after birth (for mothers)

Sensitivity of CDC 2021 STI Treatment Guidelines for diagnosis of syphilis

时间窗: from 12 weeks gestational age up to 18 months after birth

Clinical data used to diagnose syphilis according the CDC 2021 STI Guidelines will be collected as part of standard clinical care from the time of pregnancy (greater than or equal to 12 weeks gestational age) up to 18 months after birth.

Positive predictive value of CDC 2021 STI Treatment Guidelines for diagnosis of syphilis

时间窗: from 12 weeks gestational age up to 18 months after birth

Clinical data used to diagnose syphilis according the CDC 2021 STI Guidelines will be collected as part of standard clinical care from the time of pregnancy (greater than or equal to 12 weeks gestational age) up to 18 months after birth.

Negative predictive value of CDC 2021 STI Treatment Guidelines for diagnosis of syphilis

时间窗: from 12 weeks gestational age up to 18 months after birth

Clinical data used to diagnose syphilis according the CDC 2021 STI Guidelines will be collected as part of standard clinical care from the time of pregnancy (greater than or equal to 12 weeks gestational age) up to 18 months after birth.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Irene Stafford

Associate Professor

The University of Texas Health Science Center, Houston

研究点 (18)

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