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临床试验/NCT05634850
NCT05634850招募中不适用

A Pilot Study: A Prospective, Longitudinal, Observational Study, Evaluating the Usability of the Product Kinder System Trial, Home Based Hormone for In-Vitro Fertilization (IVF) Monitoring System.

Planet Innovation1 个研究点 分布在 1 个国家目标入组 25 人开始时间: 2022年9月9日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
25
试验地点
1
主要终点
To evaluate the usability of Kinder by patients undergoing controlled ovarian stimulation cycle

研究概览

简要总结

In-vitro fertilisation (IVF) treatment involves women undergoing hormone stimulation (drug dosing) to produce more oocytes (eggs) to increase their chances of fertilisation. The information that IVF clinicians currently collect on a woman's hormonal response to IVF drug dosing comes from in-clinic blood testing. This requires patients to make a visit to the IVF clinic every few days to have the blood samples taken. The blood is then analysed in a laboratory for the hormone levels and the results are then sent back to the clinic. This monitoring process of frequent onsite visits and blood draws can often be quite inconvenient and disruptive for patients.

This observational study will assess a non-invasive in vitro diagnostic (IVD) device for measuring the common fertility hormones in urine. The test system is for use by both healthcare professionals in a clinical setting and nonprofessionals in a home care setting under the guidance of a health care professional. This study will provide pilot data on the usability of the IVD device from the intended end users as well as the correlation of urinary metabolite levels as measured by the IVD device and the serum concentration as measured by blood analysers.

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
30 Years 至 40 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Women undergoing controlled ovarian stimulation treatment
  • 30 to 40 years old (inclusive)
  • Willingness to comply with study procedures for collection and testing of urine

排除标准

  • Illiterate in English
  • No access to smart phone that is compatible with App and/or is not connected to the internet
  • Patients who are diabetic (Type I and Type II), have insulin resistance or a renal/liver disorder
  • Patients who have taken oral contraceptives up to 4 days before the first stimulation day of the cycle

结局指标

主要结局

To evaluate the usability of Kinder by patients undergoing controlled ovarian stimulation cycle

时间窗: A single controlled ovarian stimulation cycle, typically up to 20 days

Patients will perform tests with the Kinder system and complete a usability questionnaire on their experience.

Correlation of fertility hormone serum and urinary metabolites

时间窗: A single controlled ovarian stimulation cycle, typically up to 20 days

Correlation of E2, P4 and LH and their urinary metabolites (E1-3G, PdG and LH)

次要结局

未报告次要终点

研究者

发起方
Planet Innovation
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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