New non-invasive method for selecting embryos in IVF
Official title: A Novel Integrative Non-invasive Embryo Selection Approach for in Vitro Fertilization Based on Artificial Intelligence Enhanced Morphokinetic Analysis and Raman Spectra in Spent Culture Media
Run by Chinese University of Hong Kong · NCT05896709 · Data updated 2026-11-12
This study is testing a new non-invasive way to choose the best embryos during IVF to see if it can help more people get pregnant.
Quick facts
| Study type | Interventional |
|---|---|
| Sex | All |
| Enrollment | 176 (estimated) |
| Sponsor | Chinese University of Hong Kong Academic / other |
| Locations | 1 site (Hong Kong) |
| Status | Recruiting |
| Started | July 17, 2023 |
| Main results expected | March 2026 |
| Study ends | December 2026 |
| Registry record updated | March 21, 2025 |
| Trial ID | NCT05896709 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include patients undergoing their first, second, or third IVF/ICSI treatment cycle with at least three normal fertilized embryos.
✕Probably not a fit
Patients with known genetic diseases or those whose embryos do not meet imaging quality standards may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study aims to improve embryo selection during in vitro fertilization (IVF) by using a novel non-invasive approach that combines morphokinetic analysis with Raman spectroscopy. In the first phase, archived data will be analyzed to train a convolutional neural network (CNN) for embryo selection. The second phase will involve a randomized controlled trial to assess the effectiveness of this integrated method in increasing clinical pregnancy rates. The approach promises to provide a quicker and more cost-effective alternative to traditional invasive genetic testing methods.
Why it matters
Potential benefit: If successful, this method could significantly enhance the chances of clinical pregnancy for patients undergoing IVF.
How similar studies have gone: Other studies have shown promise in using AI and non-invasive techniques for embryo selection, indicating a growing interest in this innovative approach.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Patients undergoing IVF/ ICSI treatment 2. Patients receiving the first, second or third IVF/ICSI treatment cycle 3. Patients and their partners willing to sign the informed consent agreement 4. Patients having at least three normal fertilised embryos on the day of the fertilization check 5. Consecutive women undergoing IVF treatment 6. Patients planning to use a time-lapse incubator for embryo culture Exclusion Criteria: 1. Day one human embryos with blur imaging 2. Large obstructions in the embryo area 3. More than half of the embryo area is blocked by the well or degeneration 4. Patients with more than half of the embryos without sufficient spent culture medium for RS analysis 5. Patients with known genetic diseases
Where it's running
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The Chinese University of Hong Kong
Hong Kong, Hong Kong Recruiting
Study contacts
- Principal investigator: Pui Wah Jacqueline Chung — Chinese University of Hong Kong
- Study coordinator: Pui Wah Jacqueline Chung
- Email: jacquelinechung@cuhk.edu.hk
- Phone: +852 35051537
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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G-CSF for DOR in women undergoing IVF
This trial tests whether G-CSF shots can improve IVF outcomes for women with diminished ovarian reserve.
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Dual Trigger vs HCG Trigger for Final Maturation in Normal Responders
In normal responders undergoing ICSI cycles, this study tests whether using a dual trigger (GnRH agonist plus hCG) improves outcomes compared with the standard hCG trigger.
-
Pentoxifylline to improve uterine lining and frozen embryo transfer outcomes
This trial sees if giving pentoxifylline alongside standard estradiol helps women with good-quality day‑5 frozen embryos get a thicker uterine lining and better frozen embryo transfer success.
-
Tadalafil to increase uterine lining and improve frozen embryo transfer success
This test sees if adding daily tadalafil to standard estrogen helps women with unexplained infertility using good-quality day‑5 frozen embryos get a thicker uterine lining and better transfer outcomes.
-
Aromatherapy to support mental health in women undergoing IVF
This will test whether inhaling lavender oil twice daily can reduce anxiety, stress, and depression and improve quality of life for women awaiting IVF.
-
AI tool to analyze sperm and predict their ability to help IVF/ICSI succeed
This project will test an AI platform that analyzes semen samples from men providing sperm for IVF/ICSI to see if it can predict which samples have the best chance of supporting successful IVF/ICSI outcomes.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.