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

StatusActive, Not Recruiting
PhaseNot applicable
Started
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Record History

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  1. Primary endpoint(s) modifiedv3 Show 4 more changesShow less
    • Trial status changed: Recruiting → Active, Not Recruiting
    • Study completion moved earlier from Jun 2027 to Sep 2026
    • Primary completion date changed from estimate of Jun 2026 to Jun 29, 2026
    • Site details revised
  2. Start date changed from estimate of Jul 2025 to Jul 27, 2025v2
  3. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
UConn Health
38 trials monitored
See 2 trials at risk
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.
Trial Details
NCT Number NCT07062237
Lead Sponsor UConn Health
Collaborators: The Center for Advanced Reproductive Services, P.C.
Conditions
(from sponsor)		 Infertility, Male Factor Infertility
Related terms Infertility
Enrollment 187 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov