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临床试验/NCT03957200
NCT03957200已完成不适用

Assessing Gestational Age in First Trimester Pregnancies: A Comparison of a New Handheld Wireless Transabdominal Ultrasound to a Portable Transabdominal Ultrasound

University of Manitoba2 个研究点 分布在 1 个国家目标入组 57 人开始时间: 2019年6月18日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
57
试验地点
2
主要终点
Can Both Transabdominal Ultrasounds See a Gestational Sac and Yolk Sac or Embryo?

研究概览

简要总结

The objective of this study is to assess equivalency of the transabdominal Clarius handheld wifi C3 ultrasound (which uses Bluetooth to locate the ipad Mini 5 and then uses wifi direct to show the images) to the current standard of care in Women's Hospital outpatient department the portable Zonare ZS3 in patients presenting in the first trimester of pregnancy.

详细描述

This is a prospective study in which first trimester participants who are presenting to discuss termination of pregnancy, will consent to have an additional transabdominal ultrasound with the Clarius C3 immediately prior to their standard ultrasound which is performed to date their pregnancy. Participants who are presenting for medical abortion have been prescreened to be estimated to be less than 9 weeks GA. Participants who are being seen prior to surgical abortion will have been screened by nurses based on their last menstrual period or estimated time of conception to estimate their gestational age. Potential participants estimated to be less than 13 weeks GA, will be approached to see if they are interested in participating in the study before they are seen by their health care provider. The name, date of approach, and reason for decline of potential participants who refuse to participate will be documented. If agreeable, the participant will complete consent with a study nurse or medical student for the additional ultrasound.

Participants will then receive the 2 ultrasounds by the same health care provider with the Clarius C3 ultrasound first, then the standard care ultrasound. Occasionally, there may be a different provider doing the Clarius C3 ultrasound when the patient consents.

Participants will receive standard care for medical or surgical abortion. The following information will be documented from their chart:

Height and weight, age, Obstetrical history (Gravida, para, number cesareans, ectopic pregnancies, spontaneous abortions, therapeutic abortions). If they do not have a documented intrauterine pregnancy, the standard questions to rule out possibility of ectopic pregnancy will be determined, and any positive answers will be documented in the chart. Anyone without a documented intrauterine pregnancy (no gestational sac or a gestational sac with no definite crown rump length or yolk sac) will be followed until a final outcome is determined or they are lost to follow up. When the patient has a pregnancy of unknown location (no evidence of a pregnancy inside or outside of the uterus), their data will not be used to compare the two ultrasounds but future outcome will be recorded.

The final outcome of their pregnancy and any complications will be determined within the next 6 weeks with the following potential outcomes:

研究设计

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

入排标准

年龄范围
12 Years 至 50 Years(Child, Adult)
性别
Female
接受健康志愿者

入选标准

  • Presenting requesting medical or surgical abortion
  • Estimated to be under 13 weeks gestational age based on last menstrual period or time of conception, or nurses best estimate.
  • Able to provide informed consent with adult supervision of a minor or with an interpreter present

排除标准

  • Unable to provide informed consent

结局指标

主要结局

Can Both Transabdominal Ultrasounds See a Gestational Sac and Yolk Sac or Embryo?

时间窗: Results will be known immediately after both ultrasounds are completed

Number of participants with both ultrasounds showing a gestational sac with a yolk sac or embryo

次要结局

  • Can Both Transabdominal Ultrasounds Give a Crown Rump Length or Gestational Sac Size to Within 5 Days(Results will be known immediately after both are completed)

研究者

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

Helen Pymar

Associate Professor

University of Manitoba

研究点 (2)

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