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临床试验/NCT02304835
NCT02304835已完成不适用

Feasibility of a Self-performed Urinary Test for the Follow-up on Medical Abortion

Nordic Pharma SAS1 个研究点 分布在 1 个国家目标入组 322 人开始时间: 2013年5月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
322
试验地点
1
主要终点
concordance between qualitative results from the urinary test and quantitative values from the beta-hCG blood measurement.

研究概览

简要总结

This study was a national, longitudinal, prospective, observational survey, carried out in metropolitan France, with a sampling of 21 birth control centres.

The aim of this study was to assess, in real life conditions, the benefit of a urinary semi-quantitative test (hCG Duo 5-1000) in the follow-up of medical abortion by analysing the concordance between qualitative results from the urinary test and quantitative values from the beta-hCG blood measurement.

研究设计

研究类型
Observational
观察模型
Cohort
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

  • Adult women (18 years old or more), pregnant the day of the medical examination and asking for medical abortion.
  • Patients agreeing to participate in the study after have been informed orally by the physician and given the information sheet.
  • Informed patients accepting the computer processing of their medical data and their right of access and correction.

排除标准

  • Patients with more than 49 Days of Amenorrhea (DA) for private practice and 63 DA for hospital practice.
  • Patients with contraindications to medical abortion.
  • Patients with severe and progressive disease.
  • Patients unable to complete a questionnaire.
  • Patients refusing to participate in the study.

结局指标

主要结局

concordance between qualitative results from the urinary test and quantitative values from the beta-hCG blood measurement.

时间窗: At the follow-up at 2-3 weeks after inclusion

There was concordance if : * The result of urinary test is \< 1000 IU/L and the value of β-hCG blood measurement was \< 1000 IU/L, Or if * The result of urinary test is ≥ 1000 iu/L and the value of β-hCG blood measurement was ≥ 1000 IU/L. There was discrepancy if: * The result of urinary test is ≥ 1000 IU/L and the value of β-hCG blood measurement was \< 1000 IU/L, Or if * The result of urinary test is \< 1000 IU/L and the value of β-hCG blood measurement was ≥ 1000 IU/L.

次要结局

  • Acceptability of the urinary semi-quantitative test by the patient(at the follow up at 2-3 weeks after the inclusion)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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