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First-Trimester Ultrasound Assessment of Velamentous Cord Insertion (1T-VCI)

2026年11月10日 更新者:Linus Lee、Hospital Authority, Hong Kong

Prospective Study of First-Trimester Ultrasound Direct Visualisation of Velamentous Cord Insertion

The goal of this observational study is to learn whether a short ultrasound assessment during the routine first-trimester pregnancy scan can identify velamentous cord insertion, an abnormal location where the umbilical cord joins the placenta. The study will include pregnant participants aged 18 years or older with a singleton pregnancy who attend first-trimester combined screening between 11+0 and 13+6 weeks of pregnancy.

The main questions it aims to answer are:

  • How often can the placental cord-insertion site be successfully classified within a 3-minute assessment?
  • How accurately does first-trimester ultrasound identify velamentous cord insertion compared with examination of the placenta after delivery?

Participants will:

  • Attend their usual first-trimester ultrasound examination.
  • Have an additional transabdominal ultrasound assessment of the placental cord-insertion site after the routine scan, taking no more than 3 minutes.
  • Allow the study team to review relevant pregnancy and birth records.
  • If they deliver at the study hospital, allow examination of the placenta after delivery as part of the study reference standard.

研究概览

地位

尚未招聘

条件

详细说明

Participants with singleton pregnancies attending first-trimester combined screening between 11+0 and 13+6 weeks will be invited to participate. The research-specific placental cord-insertion assessment will be performed after completion of routine clinical care and will not replace or alter standard ultrasound assessment. The insertion will be initially classified as normal, VCI, or undetermined.

VCI or undetermined examinations will undergo repeat ultrasound assessment in the same setting or within 1 week by maternal-fetal-medicine team, transvaginal ultrasound may be considered to facilitate visualization. If an abnormal insertion is confirmed, subsequent care, including repeat assessment and transvaginal ultrasound for vasa previa where clinically indicated, will follow existing practice.

For participants who deliver at the study hospital, available placentas will undergo blinded structured postnatal gross examination and standardized photographic documentation. The final postnatal placental classification, reviewed by an assessor blinded to antenatal ultrasound classifications and neonatal outcome, will serve as the reference standard for the primary diagnostic-accuracy analysis.

研究类型

观察性的

注册 (估计的)

1000

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

学习地点

      • Hong Kong、香港
        • Pamela Youde Nethersole Eastern Hospital

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

是的

有资格学习的性别

女性

取样方法

非概率样本

研究人群

The study population comprises pregnant participants aged 18 years or older with singleton pregnancies who attend routine first-trimester combined screening at Pamela Youde Nethersole Eastern Hospital Hong Kong between 11+0 and 13+6 weeks of gestation. Participants must have capacity to provide written informed consent. Individuals with multiple pregnancies and those who decline or withdraw consent will not be included. All enrolled participants will undergo the same focused, research-specific transabdominal ultrasound assessment of the placental cord-insertion site after completion of their routine clinical screening examination.

描述

Inclusion Criteria:

  • Pregnant participants aged 18 years or older with a singleton pregnancy
  • Attendance for first-trimester combined screening at 11+0 to 13+6 weeks
  • Capacity to provide written informed consent

Exclusion Criteria:

  • Multiple pregnancy
  • Declined or withdrawn consent

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 观测模型:COHORT
  • 时间观点:PROSPECTIVE

队列和干预

团体/队列
Singleton pregnancies undergoing first-trimester placental cord-insertion assessment

Consenting pregnant participants aged 18 years or older with singleton pregnancies attending first-trimester combined screening at Pamela Youde Nethersole Eastern Hospital Hong Kong at 11+0 to 13+6 weeks gestation. Following routine screening, participants undergo a focused transabdominal placental cord-insertion assessment of up to 3 additional minutes, with review or repeat assessment according to the prespecified pathway where needed.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Sensitivity of First-Trimester Ultrasound for Detecting Velamentous Cord Insertion
大体时间:Up to 7 months after the baseline assessment, at postnatal placental examination.

Sensitivity of first-trimester ultrasound for detection of velamentous cord insertion

Up to 7 months after the baseline assessment, at postnatal placental examination.
Specificity of First-Trimester Ultrasound for Detecting Velamentous Cord Insertion
大体时间:Up to 7 months after the baseline assessment, at postnatal placental examination.

Specificity of first-trimester ultrasound for detection of velamentous cord insertion

Up to 7 months after the baseline assessment, at postnatal placental examination.
Percentage of Participants with a Definitive Classification Within the Initial 3-Minute Ultrasound Assessment
大体时间:Baseline

Proportion of participants classified as either normal placental cord insertion or velamentous cord insertion within the prespecified 3-minute focused ultrasound assessment.

Baseline
Percentage of Participants with a Definitive Classification After Completion of the Assessment Pathway
大体时间:Up to 1 week after the baseline assessment

Proportion of participants with a final classification of either normal placental cord insertion or velamentous cord insertion after maternal-fetal-medicine review and/or repeat ultrasound assessment, where required.

Up to 1 week after the baseline assessment

次要结果测量

结果测量
措施说明
大体时间
Percentage of Participants with an Indeterminate Initial Placental Cord-Insertion Assessment
大体时间:Baseline

Proportion of participants with an indeterminate initial placental cord-insertion classification and documented reasons for indeterminate assessment, if any

Baseline
Neonatal Birth Weight
大体时间:At delivery

Birth weight recorded at delivery, and local gestational age specific centiles where available

At delivery
Gestational age at delivery
大体时间:At delivery

Gestational age in completed weeks at delivery

At delivery
Mode of delivery
大体时间:At delivery

Mode of delivery recorded from maternity records

At delivery
Neonatal Apgar Scores at 1 and 5 Minutes After Birth
大体时间:At delivery episode, 1 and 5 minutes after birth

Apgar scores assessed at 1 and 5 minutes after birth. Scores range from 0 to 10, with higher scores indicating better neonatal condition.

At delivery episode, 1 and 5 minutes after birth
NICU admission
大体时间:At delivery episode

Admission to a neonatal intensive care unit

At delivery episode

其他结果措施

结果测量
措施说明
大体时间
Hypertensive disorders of pregnancy
大体时间:From baseline assessment to delivery, up to 7 months

Incidence of gestational hypertension, pre-eclampsia, or chronic hypertension with superimposed pre-eclampsia, summarized descriptively according to antenatal and postnatal placental cord-insertion status

From baseline assessment to delivery, up to 7 months

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Linus Lee、Hospital Authority

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年11月1日

初级完成 (估计的)

2028年6月1日

研究完成 (估计的)

2028年6月1日

研究注册日期

首次提交

2026年10月23日

首先提交符合 QC 标准的

2026年11月10日

首次发布 (实际的)

2026年11月13日

研究记录更新

最后更新发布 (实际的)

2026年11月13日

上次提交的符合 QC 标准的更新

2026年11月10日

最后验证

2026年11月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

IPD 计划说明

Individual participant data will not be shared outside the study team because the study involves potentially identifiable pregnancy, ultrasound, placental, and perinatal clinical data held under institutional data-governance and privacy requirements. De-identified aggregate data may be available in publications or on reasonable request, subject to applicable approval and requirements.

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

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