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IVF lab test: when to hatch embryos for best genetic results?

NCT ID NCT07154875

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 26, 2026 · Last updated Sep 11, 2026 · Updated 4 times

Summary

This study looks at whether doing a laser-assisted hatching procedure on Day 3 or Day 5 of embryo growth changes the genetic test results in IVF. About 200 people having IVF with genetic testing will take part. The goal is to see if timing affects embryo health and the accuracy of genetic screening.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Assisted hatching (laser procedure to thin the embryo's outer shell)
What this could lead to
If it works, this could help IVF labs choose the best timing for assisted hatching to improve embryo selection and genetic testing accuracy.
What could go wrong
This is a small, early-stage trial focused on lab outcomes, not pregnancy or live birth. The results may not directly improve success rates for patients.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

141 people

The number who actually took part.

Started

Jun 2025

Finished

Jul 2026

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 years and older

Sex

Female participants only

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Female participants undergoing IVF-ICSI with an indication for PGT-A * Age ≥18 years; no prespecified upper age limit. Age was recorded for subsequent analyses * Anti-Müllerian hormone (AMH) level ≥1.0 ng/mL * Antral follicle count (AFC) ≥5 follicles * Controlled ovarian stimulation using an antagonist or progestin-primed ovarian stimulation (PPOS) protocol * Use of ejaculated sperm prepared by density-gradient centrifugation or swim-up * Written informed consent for participation Exclusion Criteria: * History of ≥3 failed IVF cycles or ≥3 consecutive miscarriages * Indication for PGT-M or PGT-SR, including monogenic disorders or structural chromosomal rearrangements * Severe uncontrolled medical or autoimmune conditions considered likely to affect oocyte or embryo development * No metaphase II (MII) oocytes available for ICSI * Use of surgically retrieved sperm * Use of advanced sperm-selection techniques, including IMSI, PICSI, or MACS * Polycystic ovary syndrome diagnosed according to the Rotterdam criteria

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Center for Reproductive Support, 16A Ha Dong General Hospital

    Hanoi, Hanoi, 100000, Vietnam