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NCT07062237 · ClinicalTrials.gov registry record · NA

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

A NA study of Infertility and Male Factor Infertility, sponsored by UConn Health.

Recruiting
Registry status
NA
Development phase
187
Enrollment target
1
Study location

NCT07062237 is a NA study of Infertility and Male Factor Infertility that is actively recruiting participants, run by UConn Health. The registered enrollment target is 187 participants, below the 7,587-participant average among 74 other Infertility trials with a reported enrollment target (98% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT07062237, a NA study of Infertility and Male Factor Infertility, is actively recruiting participants, sponsored by UConn Health.

RECRUITING
Registry status
NA
Development phase
187 participants
Enrollment target
1
Study location

Study Summary

This research is being done to determine if producing sperm after an ultrashort period of abstinence (1 hour of abstinence) will be effective in improving the rates of embryos with normal chromosomes (structures that carry genetic information) during in vitro fertilization (IVF) treatment. The investigators hypothesize that a shorter period of abstinence is effective at improving rates of normal chromosomes among embryos.

Interventions

  • OTHER Ultrashort abstinence
  • OTHER Standard abstinence

Study Locations (1)

Connecticut

  • The Center for Advanced Reproductive Services, P.C. - Farmington

Trial Details

FieldValue
Enrollment Target 187 participants
Start Date 2025-07
Est. Completion 2027-06
Phase NA

Sponsor

UConn Health

178 total trials

What the Registry Record Tells You About NCT07062237

The ClinicalTrials.gov registry entry for NCT07062237 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 187 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 7,587-participant average among 74 other Infertility trials with a reported enrollment target (98% lower). The listed sponsor is UConn Health, which has 178 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Infertility appearing as the primary indexed condition, and to 2 interventions - of which Ultrashort abstinence is the first listed.

NCT07062237 reports 1 study location spanning 1 distinct geographic area - top geographies include Connecticut.

Frequently Asked Questions

What is clinical trial NCT07062237 about?

NCT07062237 is a clinical study titled "A Randomized Clinical Trial Comparing Embryo Euploidy Rates Following Ultrashort Versus Standard Abstinence". This research is being done to determine if producing sperm after an ultrashort period of abstinence (1 hour of abstinence) will be effective in improving the rates of embryos with normal chromosomes (structures that carry genetic information) during in vitro fertilization (IVF) treatment. The inves...

What is the current status of trial NCT07062237?

This trial is currently recruiting. It is a NA study. The enrollment target is 187 participants. The study started on 2025-07. Estimated completion is 2027-06.

What conditions does trial NCT07062237 study?

This clinical trial studies the following conditions: Infertility, Male Factor Infertility.

What interventions are being tested in trial NCT07062237?

The interventions under investigation include: Ultrashort abstinence (OTHER), Standard abstinence (OTHER).

Who is sponsoring clinical trial NCT07062237?

This trial is sponsored by UConn Health, which has 178 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07062237 being conducted?

This trial has 1 study location across Connecticut. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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