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Salivary Diagnostic Testing for IVF

B

Boston IVF

Status

Completed

Conditions

Infertility

Study type

Observational

Funder types

Other

Identifiers

NCT02040545
20092198

Details and patient eligibility

About

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

Full description

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.

Enrollment

335 patients

Sex

Female

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

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

Trial design

335 participants in 1 patient group

Infertility
Description:
Patients undergoing ovulation induction and controlled ovarian hyperstimulation at a participating infertility center

Trial contacts and locations

8

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Data sourced from clinicaltrials.gov

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