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临床试验/NCT05642637
NCT05642637招募中不适用

Biobank Cycle Collection Study From Women Trying to Conceive

SPD Development Company Limited2 个研究点 分布在 1 个国家目标入组 1,500 人开始时间: 2022年12月6日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
1,500
试验地点
2
主要终点
Collection of daily urine samples from women trying to conceive

研究概览

简要总结

This study will provide daily urine samples from volunteers who are trying to conceive in order to maintain the SPD biobank.

Study volunteers, seeking to conceive will be provided with a CE marked Clearblue Ovulation product to help them pinpoint their most fertile time and aid conception. All volunteers will provide daily early morning urine samples throughout the study period and keep a study diary of menses and pregnancy test results for up to 3 menstrual cycles.

Urine samples will be received in the clinical laboratory and aliquoted and stored at -80˚C until required.

详细描述

The purpose if this study is to maintain the SPD Biobank with urine samples from cycles in which conception occurred and ones where conception did not occur, together with associated sample information including demographic and clinical data e.g. menses days, volunteer age and reproductive hormone concentrations.

Study volunteers, seeking to conceive will be recruited to the study after providing written informed consent. All volunteers will be provided with a CE marked Clearblue Ovulation product to help them pinpoint their most fertile time and aid conception and be required to collect daily early morning urine samples throughout the study until pregnancy is confirmed or their next menstrual period starts. Volunteers will be required to keep a daily diary of menses, sample collection and pregnancy test results. The study will last for up to 3 consecutive menstrual cycles if not pregnant and up to sample day 60 if pregnant.

Urine samples will be received in the clinical laboratory and will be tested for the presence of hormones related to pregnancy and fertility, then aliquoted and stored in the SPD Biobank at -80˚C until required for product development or evaluation purposes.

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

  • Females aged 18 and over actively trying to conceive
  • At least 2 regular consecutive cycles since last pregnancy/miscarriage/ stopping breastfeeding or contraception
  • Willing to disclose their pregnancy status and provide urine samples.
  • Willing to give informed consent and comply with the study procedures

排除标准

  • Trying to conceive for >6 months (under 35 years) or > 3 months (35 years and over)
  • Has a diagnosis of Polycystic Ovary Syndrome (PCOS)
  • Taking medication or has known condition which means they should not get pregnant.
  • Currently pregnant or breastfeeding
  • Using any treatment which may affect the menstrual cycle (e.g. contraceptive pill)
  • Using or has previously used infertility medications or hormone replacement medications containing LH or hCG \ (e.g. Pregnyl®)
  • Using or undergoing any other medical treatment for fertility such as ovulation drugs, artificial insemination and assisted fertility such as IVF or ICSI
  • Peri-or post-menopausal, e.g. experiencing symptoms: irregular menstrual periods, hot flushes, night sweats, sleep disturbances and/or moods swings
  • Abnormal liver or kidney function
  • Taking antibiotics containing tetracycline.
  • Participated in this study within the last 6 months

结局指标

主要结局

Collection of daily urine samples from women trying to conceive

时间窗: From recruitment until sample collection complete (up to 3 menstrual cycles if not pregnant and sample day 60 if pregnant)

Daily samples collected throughout the cycle in which conception occurs

Collection of daily urine samples from women trying to conceive

时间窗: 3 years

Daily samples collected throughout the cycle in which conception occurs

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (2)

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