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Clinical Trial Summary

This proof of concept study is designed to determine the practicality of using home ovulation tests to enable optimum timing for transfer of frozen embryos in a natural menstrual cycle in comparison to the standard ultrasound and serum monitoring currently conducted by many IVF clinics.


Clinical Trial Description

The study will evaluate the ability of home ovulation tests to accurately time Frozen Embryo Transfer (FET) directly compared to standard clinical procedures. In addition, women's likability and stress associated with timing a FET cycle using both methods will be evaluated by collecting qualitative data using standardised questionnaires. The impact of psychological stress on FET outcome such as implantation rates and viability at first scan will be considered in order to gather information for the design of a larger clinical study and basic financial data will also be collected, in order to pilot a cost-effectiveness evaluation of the two FET timing methods. A subset of volunteers will collect daily urine samples from day after embryo transfer until confirmation of pregnancy. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03156374
Study type Interventional
Source SPD Development Company Limited
Contact
Status Completed
Phase N/A
Start date April 30, 2017
Completion date September 30, 2019

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