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Trial details imported from

For full trial details, please see the original record at

Registration number
Ethics application status
Date submitted
Date registered
Date last updated

Titles & IDs
Public title
Timing Frozen Embryo Transfer by Following Two Different Methods
Scientific title
Proof of Concept Study To Assess Women's Likability and Stress in Timing Frozen Embryo Transfer by Following Two Different Methods
Secondary ID [1] 0 0
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Fertility Disorders 0 0
Condition category
Condition code

Study type
Description of intervention(s) / exposure
Treatment: Devices - Test use

Experimental: Ovulation test use - Use of both ovulation tests and standardised care

Treatment: Devices: Test use
Use of home ovulation test to predict ovulation

Intervention code [1] 0 0
Treatment: Devices
Comparator / control treatment
Control group

Primary outcome [1] 0 0
Proportion of volunteers where ADOT use enables equivalent timing of FET compared to clinic visit - Examination as to whether using ADOT would have enabled correct timing of FET when compared to clinic visit
Timepoint [1] 0 0
9 months
Secondary outcome [1] 0 0
Measurement of women's psychological distress - Use of validated questionnaire to assess stress level
Timepoint [1] 0 0
9 months
Secondary outcome [2] 0 0
Positive and negative experience in using ovulation tests in FET - Qualitative assessment of women's FET treatment experience when using ADOT compared to standard clinical procedures during the study via a semi-structured interview following embryo transfer
Timepoint [2] 0 0
9 months
Secondary outcome [3] 0 0
FET success - Implantation rate
Timepoint [3] 0 0
9 months

Key inclusion criteria
- Women aged 24 to 45 years of age

- Undergoing no more than 5frozen embryo transfer

- Average cycle length between 26 and 35 days

- Willing to provide written informed consent to participate in the study and comply
with all study procedures
Minimum age
24 Years
Maximum age
45 Years
Can healthy volunteers participate?
Key exclusion criteria
- More than five IVF frozen embryo cycle

- Undergoing FET following cancer treatment

- Self-reported drug or alcohol dependency

- Self-reported history of depression, anxiety and panic attacks

Study design
Purpose of the study
Allocation to intervention
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?

Intervention assignment
Single group
Other design features
Not Applicable
Type of endpoint(s)
Statistical methods / analysis

Recruitment status
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Date of last participant enrolment
Date of last data collection
Sample size
Accrual to date
Recruitment in Australia
Recruitment state(s)
Recruitment hospital [1] 0 0
IVFAustralia - Bondi Junction - Bondi Junction
Recruitment postcode(s) [1] 0 0
NSW 2022 - Bondi Junction

Funding & Sponsors
Primary sponsor type
Commercial sector/Industry
SPD Development Company Limited

Ethics approval
Ethics application status

Brief 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
Trial website
Trial related presentations / publications
Public notes

Principal investigator
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for scientific queries

Summary results
For IPD and results data, please see