跳至主要内容
临床试验/NCT02040545
NCT02040545已完成不适用

Venopuncture-Free IVF: Can "Patient-friendly" Salivary Hormone Measurements Replace Serum Monitoring of IVF Patients?

Boston IVF6 个研究点 分布在 1 个国家目标入组 335 人开始时间: 2010年5月21日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
Boston IVF
入组人数
335
试验地点
6
主要终点
Equivalence of Salivary Steroid Monitoring to Blood Based Monitoring

研究概览

简要总结

This study aims to determine the performance of a salivary hormone competitive immunoassay for monitoring patients during treatment for infertility.

详细描述

The goal of this study is to determine the performance of a salivary hormone competitive immunoassay for monitoring patient estrogen and progesterone levels during treatment for infertility using controlled ovarian stimulation (COH) and in vitro fertilization (IVF). Specifically, inter- and intra-assay precision, correlation with serum measurements (the gold-standard), and user satisfaction will be determined. Ultimately, the potential applicability and reliability of salivary steroid monitoring in IVF cycles will be assessed.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

入排标准

性别
Female
接受健康志愿者

入选标准

  • Patients undergoing In Vitro Fertilization (IVF) at a participating infertility center

排除标准

  • 未提供

结局指标

主要结局

Equivalence of Salivary Steroid Monitoring to Blood Based Monitoring

时间窗: 1 month

The potential applicability and reliability of salivary steroid monitoring during infertility treatment will be measured as a progression during a patient's IVF stimulation cycle. Concurrent saliva and blood draw measurements of Estradiol and Progesterone will be taken between 3-5 times during a 2-week monitoring period. Equivalence will be determined by the matched progression of Estradiol and progesterone levels (pg/ml) in the same patient at the concurrent times. Saliva Estradiol and Progesterone levels are of a magnitude of 100-200 less than serum based values and are converted using an algorithm to adjust to serum equivalence. Matched T-test will be used to test the hypothesis that the two methods are not statistically different.

次要结局

未报告次要终点

研究者

发起方
Boston IVF
申办方类型
Other
责任方
Principal Investigator
主要研究者

Alison Zimon

Reproductive Endocrinologist

Boston IVF

研究点 (6)

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