Actively Recruiting

Phase Not Applicable
Age: 18Years - 42Years
All Genders
ID07062237

A Double-Blinded Prospective Randomized Clinical Trial Comparing Euploidy Rates Among Embryos Created From Sibling Oocytes Exposed to Sperm After Ultrashort Abstinence Compared With Standard Abstinence

Led by UConn Health · Updated on 2026-04-21

187

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

Sponsors

U

UConn Health

Lead Sponsor

T

The Center for Advanced Reproductive Services, P.C.

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are investigating whether producing sperm after a very short abstinence period of just 1 hour can improve the rates of embryos with normal chromosomes during in vitro fertilization (IVF) treatment. The study aims to compare this ultrashort abstinence with the current standard abstinence period of 2 to 5 days to see if it leads to better embryo quality and pregnancy outcomes. This research is focused on couples experiencing infertility, particularly male factor infertility, and is sponsored by UConn Health. Participants will provide two sperm samples on the day of egg retrieval: one after the standard 2-5 days of abstinence and another after only 1 hour of abstinence. Their eggs will be randomly divided into two groups, with half fertilized using sperm from the standard abstinence sample and the other half fertilized using sperm from the ultrashort abstinence sample. Both groups will be part of the IVF process involving insemination or injection of sperm into the eggs. The study will assess embryo chromosome normality and other IVF outcomes. During the study, participants will undergo egg retrieval and fertilization procedures, with close monitoring of embryo development. Researchers will evaluate the rate of chromosomally normal embryos within 2 to 4 weeks of the IVF cycle, as well as pregnancy rates after embryo transfer, fertilization rates, and blastulation rates. Participation lasts through these IVF cycle stages, with data collected to understand how sperm abstinence timing affects embryo quality and pregnancy chances.

CONDITIONS

Brief Title

A Randomized Clinical Trial Comparing Embryo Euploidy Rates Following Ultrashort Versus Standard Abstinence

Who Can Participate

Age: 18Years - 42Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Nonpregnant females aged 18 to 42 years
  • At least 6 mature oocytes for ICSI or at least 8 oocytes for standard insemination at egg retrieval
  • Using standard insemination or ICSI for fertilization
  • Undergoing PGT-A (aneuploidy testing) or PGT-M (monogenic disorder testing)
  • Willing to comply with study procedures and provide informed consent
Not Eligible

You will not qualify if you...

  • Using donor oocytes, donor sperm, or gestational carrier
  • Diagnosis of cryptozoospermia (no sperm in fresh semen sample)
  • Using surgically retrieved sperm (e.g., TESA or MESA)
  • Using frozen/thawed sperm or frozen/thawed oocytes
  • Undergoing PGT-SR (structural rearrangement testing)
  • Undergoing day 3 (cleavage stage) embryo transfer
  • Having fewer than 6 mature oocytes for ICSI or fewer than 8 for standard insemination
  • Choosing to fertilize fewer than 6 oocytes for ICSI or fewer than 8 for standard insemination
  • Male partner unable to provide second semen sample within 3 hours of first
  • Male partner has an infectious disease

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 1 day

Participants produce two semen samples on the day of egg retrieval after different abstinence periods. Half of the eggs are fertilized with sperm from standard abstinence (2-5 days) and the other half with sperm from ultrashort abstinence (1 hour).

1 visit (in-person) on egg retrieval day

Follow-up

Duration - Up to 4 weeks

Participants are followed to assess embryo development and pregnancy outcomes after embryo transfer.

1 to 2 visits within 2-4 weeks after IVF cycle

Trial Site Locations

Total: 1 location

1

The Center for Advanced Reproductive Services, P.C.

Farmington, Connecticut, United States, 06032

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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