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Trial registered on ANZCTR
Registration number
ACTRN12613000953730
Ethics application status
Approved
Date submitted
23/08/2013
Date registered
27/08/2013
Date last updated
10/03/2016
Type of registration
Prospectively registered
Titles & IDs
Public title
Comparison of the performance of two sperm preparation methods for conventional in vitro fertilisation (IVF) insemination by assessing subsequent embryo development with time-lapse technology
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Scientific title
Morphokinetic analysis of embryos resulting from different sperm preparation methods (Swim-up vs Density gradient centrifugation)- a sibling oocyte study
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Secondary ID [1]
283058
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Nil
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Infertility
289898
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Condition category
Condition code
Reproductive Health and Childbirth
290262
290262
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0
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Fertility including in vitro fertilisation
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Swim-up (SU) and Density Gradient centrifugation (DGC) are both routinely used sperm preparation methods during IVF procedure. SU involves layering semen sample and culture media, and active swimming-up of sperm into the media phase so that sperm with good motility can be yielded. However there is a risk that seminal components migrate into the media which is believed to impact fertilisation and subsequent embryo growth. DGC involves centrifugations to force the motile sperm to go through density gradient media and then get separated. But centrifugations are proven to be harmful to sperm integrity and in turn affect fertilisation and subsequent embryo development. DGC is currently used as standard method for sperm preparation at Fertility North and will be used as control group. SU will be the treatment group.
Sibling oocytes collected from each participating patient will be randomly allocated into DGC (control) and SU (treatment) groups. Semen sample provided by the male partner will be split and go through different preparation methods separately. Oocytes in each group will be inseminated with sperm prepared by according method. After insemination, comparisons will be made on ferilisation rate, time post insemination to reach syngamy, 2,3,4,5,6,7,8-cell stages (t2,t3,t4,t5,t6,t7,t8)(hours), and implantation results after transfer of embryos. Only one-off intervention is involved at the sperm/egg level, none at the patient level.
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Intervention code [1]
287780
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Treatment: Other
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Comparator / control treatment
Swim-up (SU) and Density Gradient centrifugation (DGC) are both routinely used sperm preparation methods during IVF procedure. SU involves layering semen sample and culture media, and active swimming-up of sperm into the media phase so that sperm with good motility can be yielded. However there is a risk that seminal components migrate into the media which is believed to impact fertilisation and subsequent embryo growth. DGC involves centrifugations to force the motile sperm to go through density gradient media and then get separated. But centrifugations are proven to be harmful to sperm integrity and in turn affect fertilisation and subsequent embryo development. DGC is currently used as standard method for sperm preparation at Fertility North and will be used as control group. SU will be the treatment group.
Sibling oocytes collected from each participating patient will be randomly allocated into DGC (control) and SU (treatment) groups. Semen sample provided by the male partner will be split and go through different preparation methods separately. Oocytes in each group will be inseminated with sperm prepared by according method. After insemination, comparisons will be made on ferilisation rate, time post insemination to reach syngamy, 2,3,4,5,6,7,8-cell stages (t2,t3,t4,t5,t6,t7,t8)(hours), and implantation results after transfer of embryos. Only one-off intervention is involved at the sperm/egg level, none at the patient level.
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Control group
Active
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Outcomes
Primary outcome [1]
290289
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Fertilisation rate(%),
= (number of oocyte normally fertilised)/(number of oocyte inseminated)x100%
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Assessment method [1]
290289
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Timepoint [1]
290289
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24 hrs
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Primary outcome [2]
290290
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Time post insemination to reach syngamy, 2,3,4,5,6,7,8-cell stages (t2,t3,t4,t5,t6,t7,t8)(hours)
Embryoscope is a time-lapse photographing incubator providing accurate timings for biological events during embryo development. Timings for syngamy and t2,t3,t4,t5,t6,t7,t8 of embryos cultured in the Embryoscope will be automatically recorded.
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Assessment method [2]
290290
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Timepoint [2]
290290
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72 hrs
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Primary outcome [3]
290331
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Synchronity of cleavage: s2 and s3 (hours)
S2=t4-t3
S3=t8-t5
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Assessment method [3]
290331
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Timepoint [3]
290331
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72 hrs
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Secondary outcome [1]
304245
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Embryo implantation rate (%) after transfer
Implantation is confirmed by detection of fetal heart beat under ultrasound 5 weeks after oocyte pick-up.
Implantation rate (%) = (number of fetal heart beat detected)/(number of embryo transferred) x 100%
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Assessment method [1]
304245
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Timepoint [1]
304245
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5 weeks
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Eligibility
Key inclusion criteria
All patients who meet the IVF treatment criteria according to Fertility North protocols, including tubal factor, PCOS, low AMH or multiple failures in previous IUI treatment.
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Minimum age
18
Years
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Maximum age
45
Years
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Sex
Females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Semen quality of partner not within normal range
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Non-randomised trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
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Who is / are masked / blinded?
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Intervention assignment
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Other design features
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Phase
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Type of endpoint/s
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Statistical methods / analysis
Data collected will udergo t-tests. so the number of participants was calculated via an on-line sample size calculator.
http://www.statstodo.com/SSiz2Means_Pgm.php
Fixed setting: Probability of Type I Error (a) = 0.05 &
Power (1 - B) = 0.8.
Regarding the (Difference to be detected) and (Within group SD), different values were used for different parameters. The final sample size (n=180 for each group) was determined by the biggest sample size required for any parameters to be assessed.
The average egg number collected per patient at Fertility North is 6, so the estimated number of participants is 60
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Recruitment
Recruitment status
Withdrawn
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Reason for early stopping/withdrawal
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Date of first participant enrolment
Anticipated
1/11/2013
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Actual
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
60
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
WA
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Funding & Sponsors
Funding source category [1]
287822
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Commercial sector/Industry
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Name [1]
287822
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Fertility North
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Address [1]
287822
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Suite 213, Specialist Medical Centre
Joondalup Health Campus
Shenton Ave
Joondalup WA 6027
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Country [1]
287822
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Australia
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Primary sponsor type
Commercial sector/Industry
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Name
Fertility North
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Address
Suite 213, Specialist Medical Centre
Joondalup Health Campus
Shenton Ave
Joondalup WA 6027
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Country
Australia
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Secondary sponsor category [1]
286552
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University
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Name [1]
286552
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Edith Cowan University
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Address [1]
286552
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270 Joondalup Drive,
Joondalup WA 6027
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Country [1]
286552
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
289769
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Joondalup Health Campus Human Research Ethics Committee
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Ethics committee address [1]
289769
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Joondalup Health Campus, Shenton Ave, Joondalup, WA 6027
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Ethics committee country [1]
289769
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Australia
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Date submitted for ethics approval [1]
289769
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02/09/2013
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Approval date [1]
289769
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20/09/2013
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Ethics approval number [1]
289769
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1319
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Summary
Brief summary
Both Swim-up and Density gradient centrifugation are routine sperm preparation methods in IVF laboratory. However the content of seminal fluid might mix with separated sperm in the Swim-up method while centrifugation is involved in the other method which are both considered harmful to fertilisation and embryo development. The proposed study will use time-lapse technology to reveal the differeces in the subsequent embryo development.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
42326
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Mr Yanhe Liu
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Address
42326
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Fertility North
Suite 213, Specialist Medical Centre, Joondalup Health Campus, Shenton Ave, Joondalup WA 6027
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Country
42326
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Australia
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Phone
42326
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+61 8 9301 1075
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Fax
42326
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Email
42326
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[email protected]
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Contact person for public queries
Name
42327
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Phill Matson
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Address
42327
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Fertility North
Suite 213, Specialist Medical Centre, Joondalup Health Campus, Shenton Ave, Joondalup WA 6027
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Country
42327
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Australia
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Phone
42327
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+61 8 9301 1075
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Fax
42327
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Email
42327
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[email protected]
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Contact person for scientific queries
Name
42328
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Phill Matson
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Address
42328
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Fertility North
Suite 213, Specialist Medical Centre, Joondalup Health Campus, Shenton Ave, Joondalup WA 6027
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Country
42328
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Australia
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Phone
42328
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+61 8 9301 1075
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Fax
42328
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Email
42328
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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