Sperm sorting showdown: can a microchip pick the best sperm for pregnancy?
NCT ID NCT05693220
First seen Sep 15, 2026 · Last updated Sep 16, 2026 · Updated 1 time
Summary
Researchers at the University of California, San Francisco, are comparing two ways to prepare sperm before intrauterine insemination (IUI). One method uses a microfluidic device called Zymot Multi to sort sperm, while the other uses density gradient centrifugation, a standard lab technique. The trial will enroll 270 women under 41 who are having IUI for the first time with partner sperm. The goal is to see which method leads to more clinical pregnancies over multiple IUI cycles.
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 using the Zymot Multi device
- What this could lead to
- If microfluidic sorting works better, it could become a preferred method for preparing sperm before IUI, potentially improving pregnancy rates for couples with infertility.
- What could go wrong
- This is a single-center study with 270 participants, so results may not apply to everyone. The method might not improve pregnancy rates, and it could be more expensive or technically difficult to implement widely.
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
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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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About 270 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Feb 2023
- Expected to finish
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Dec 2027
An estimate. End dates often move.
- 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 years and older
- Sex
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Anyone
- Healthy volunteers
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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 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: * Patients undergoing intrauterine insemination * Patient assigned female at birth with age \<41 Exclusion Criteria: * Any significant disease or psychiatric disorder that would interfere with the consenting process * Prior intrauterine insemination * Use of frozen donor sperm * Non-English speaker
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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UCSF Center for Reproductive Health
RECRUITINGSan Francisco, California, 94158, United States
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- Could freezing sperm outsmart father time?