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临床试验/NCT06893484
NCT06893484进行中(未招募)不适用

Assessing Completion of Medication Abortion for Very Early Pregnancies

University of Washington5 个研究点 分布在 1 个国家目标入组 400 人开始时间: 2025年3月13日最近更新:

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
400
试验地点
5
主要终点
Proportion of participants with negative high-sensitivity urine pregnancy test at 2 weeks

研究概览

简要总结

This is a prospective study to evaluate if successful completion of a medication abortion in patients with very early pregnancy can be detected with a urine pregnancy test at 2 weeks instead of 4 weeks. Additionally, the resolution of pregnancy symptoms in these patients will be characterized. Enrolled participants will take take weekly pregnancy tests and complete weekly questionnaires on their pregnancy symptoms for 4 weeks after their medication abortion.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

性别
Female
接受健康志愿者

入选标准

  • Pregnant person with early pregnancy ≤42 days
  • Eligible and consented to a medication abortion
  • Have access to receiving text messages and the internet
  • Able to read and understand English

排除标准

  • - Privacy or safety concerns about filling out the surveys

结局指标

主要结局

Proportion of participants with negative high-sensitivity urine pregnancy test at 2 weeks

时间窗: From time of taking Mifepristone to negative pregnancy test or 4-5 weeks of questionnaires

To estimate the proportion of negative high-sensitivity urine pregnancy tests in participants with very early pregnancy and a complete abortion at 2 weeks after taking Mifepristone and compare this proportion to the proportion of negative high-sensitivity urine pregnancy tests in participants with very early pregnancy and a complete abortion at 4 weeks

次要结局

  • Time to resolution of pregnancy symptoms(From time of taking Mifepristone to negative pregnancy test or 4-5 weeks of questionnaires)

研究者

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

Lyndsey Benson

Assistant Professor, Obstetrics & Gynecology

University of Washington

研究点 (5)

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