A Randomized Clinical Trial Comparing Embryo Euploidy Rates Following Ultrashort Versus Standard Abstinence
Part of paid clinical trials in Farmington, Connecticut.
- Sponsor
- UConn Health
- Study ID
- NCT07062237
- Status
- Recruiting
Conditions
- Infertility
- Male Factor Infertility
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 42 Years
- Healthy Volunteers
- Not accepted
Interventions
- Ultrashort abstinence — OTHERUltrashort abstinence: producing a sperm sample after 1 hour of abstinence.
- Standard abstinence — OTHERStandard abstinence: producing a sperm sample after 2-5 days of abstinence.
Study Details
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.
Key Dates
- Start date
- Jul 27, 2025
- Status verified
- Jun 2025
- Primary completion
- Jun 30, 2026
- Completion
- Jun 30, 2027
Study Design
- Enrollment
- 187 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Ultrashort abstinenceHalf of participants eggs will be exposed to sperm produced after ultrashort abstinence (1 hour of abstinence).
- Active Comparator: Standard abstinenceHalf of participants eggs will be exposed to sperm produced after standard abstinence (2-5 days of abstinence).
Primary Outcome Measure
Euploidy rate per oocyte [ Time Frame: Within 2-4 weeks of IVF cycle ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| The Center for Advanced Reproductive Services, P.C. | Farmington | Connecticut | 06032 | Lawrence Engmann, MD; MRCOG (PRINCIPAL_INVESTIGATOR) |
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