New chip could pick healthier sperm for IVF
NCT ID NCT03085433
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a microfluidic chip that gently separates healthy, motile sperm from semen without harsh chemicals. Researchers compared it to the standard spinning method in 393 couples undergoing IVF for unexplained infertility. The goal was to see if the chip leads to higher-quality embryos on day 3 of development.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Microfluidic sperm sorting device
- What this could lead to
- If successful, this device could become a standard, gentler way to select sperm for IVF, potentially improving embryo quality and pregnancy chances.
- What could go wrong
- This is a completed trial, but the improvement in embryo quality may not translate into higher live birth rates. The device may not work for all types of male infertility.
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
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393 people
The number who actually took part.
- Started
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Jun 2017
- Finished
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Apr 2022
- Lead sponsor
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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
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18 to 65 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide 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: * The target population includes couples planning in vitro fertilization (IVF) with intracytoplasmic sperm injection (ICSI). * Subjects with and without a history of prior IVF cycles will be included. * All eligible couples where both partners are \>=18 years of age will be asked to join the study. Exclusion Criteria: * Male partner with severe oligoasthenospermia (concentration \< 5 x 10\^6 spermatozoa/mL; motility\< 10%) * Female partner with anovulation (PCOS, FHA) * Female partner age \>41 * Female partner AFC\< 7 * Female partner with obstructed fallopian tubes (assessed in all patients prior to IVF) * Use of oocyte donor * Either Partner: * Cancer diagnosis in either partner * Any significant disease or psychiatric disorder that would interfere with consenting process * Treatment History: o History of \>1 prior cycle cancellation due to poor response * Treatment Plan: * Embryo co-culture * Use of adjunctive non-gonadotropin medications to improve embryo quality: growth hormone, sildenafil
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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
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University of California San Francisco
San Francisco, California, 94158, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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