What To-be-discard Biomaterials From ART Cycles Can Tell us About the Treatment Cycle Outcome?
1 other identifier
observational
50
1 country
1
Brief Summary
Various to-be-discard material from IVF treatment cycle will be collect and examined, aiming to identify potential reasons of successful outcome or cycle failure.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Jul 2023
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
July 4, 2023
CompletedFirst Submitted
Initial submission to the registry
August 23, 2023
CompletedFirst Posted
Study publicly available on registry
September 1, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
June 1, 2027
September 1, 2023
August 1, 2023
3.4 years
August 23, 2023
August 28, 2023
Conditions
Outcome Measures
Primary Outcomes (2)
DNA/RNA sequencing data
DNA / RNA analysis including the length and the quantity, RNA-seq will be applied for transcriptome profiling. Next generation sequencing will be performed to determine the sequence of DNA/RNA for our collected samples.
Through study completion, around 3 year
Proteomic profile
Protein profile will be investigated in a pool sample, treated samples will go for mass spectrometry (MS) data acquisition and finally destined for data analysis and interpretation.
Through study completion, around 3 year
Secondary Outcomes (3)
Blastocyst formation rate
5 days after fertilization
Clinical pregnancy rate
Around 5 weeks after embryo transfer
Live birth rate
Around 9 months after embryo transfer
Eligibility Criteria
Study population will include patients attending the Assisted Reproductive Technolohy (ART) Unit of the Chinese University of Hong Kong for ART treatment.
You may qualify if:
- Patients attending the Assisted Reproductive Technology (ART) Unit of the Chinese University of Hong Kong for ART treatment.
- Participant able to give voluntary, written, informed consent to participate in the study.
You may not qualify if:
- Patient using donor gamete in IVF treatment
- Patient refuses to join and failed to giving consent for any reasons
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
The Chinese University of Hong Kong and Prince of Wales Hospital
Hong Kong, Hong Kong
Biospecimen
IVF cycle to-be-discard biomaterials including follicular fluid, seminal plasma, immature oocytes, abnormal fertilized zygote, unfertilized zygote, arrested embryos, poor quality blastocysts, spent culture medium.
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Yiu Leung D Chan, DPhil
CUHK
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assited Professor
Study Record Dates
First Submitted
August 23, 2023
First Posted
September 1, 2023
Study Start
July 4, 2023
Primary Completion (Estimated)
December 1, 2026
Study Completion (Estimated)
June 1, 2027
Last Updated
September 1, 2023
Record last verified: 2023-08