IVF Outcomes

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Review clinical trials related to IVF Outcomes. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Development of an AI Platform for the Analysis of Sperm and Prediction of Their Clinical Potential

Prospective, multicenter research study with a split-sample design on semen samples, without intervention, to develop an artificial intelligence platform for the analysis of sperm samples and prediction of their clinical potential, in 500 semen samples, in an in vitro study over 24 months.

Participants needed: 500
Trial details
Age: 18-60Biological sex: AllType: ObservationalSponsor: Fecundis Lab SLUpdated: Jun 12, 2026Locations: 5
Eligibility criteria

Ability to provide a semen sample via masturbation [+1]

Current diagnosis of a sexually transmitted infection (STI) [+6]

Status: Recruiting

HELIOS Advanced: Human Oocyte Illumination to Enhance Development

Oocytes need a lot of energy to complete meiosis and fertilize successfully. As women get older, the "power plants" of the cells (called mitochondria) don't work as well. This makes it harder for eggs and embryos to develop normally. One possible way to help is with a gentle light treatment called photobiomodulation (PBM). This uses a special type of red light that boosts energy production in cells and helps them stay healthy. This study will test whether adding this light treatment during in vitro fertilization (IVF) can improve embryo growth and pregnancy outcomes.

Participants needed: 270
Trial details
Age: 18-48Biological sex: FemaleType: InterventionalSponsor: Columbia UniversityUpdated: Mar 25, 2026Locations: 1
Eligibility criteria

Female age between 18-48 years at the time of the IVF/ICSI cycle [+5]

Use of donor oocytes or gestational carrier [+2]

Status: Recruiting

Ovarian Stimulation Outcomes During a GnRH Antagonist Protocol for In-vitro Fertilization When Comparing Trigger Day Decision by Physicians Versus an Artificial Intelligence-based Algorithm.

To compare the number of mature oocytes following a GnRH antagonist in-vitro fertilization stimulation cycle when comparing trigger day timing decision by physicians versus an artificial intelligence-based algorithm

Participants needed: 180
Trial details
Age: 18-45Biological sex: AllType: InterventionalSponsor: FertilAIUpdated: Jan 12, 2026Locations: 1
Eligibility criteria

All patients undergoing an ovarian stimulation cycle utilizing the GnRH antagoni...

Loss to follow-up, patient retracts consent to participate

Status: Recruiting

The Effect of VitC on IVF Outcome of DOR Patients

In the context of the accelerating aging population and the continuous decline in birth rates nationwide, delaying reproductive aging in women and protecting the fertility of women of childbearing age have become urgent issues and key demands that need to be addressed in the field of maternal and child health in China. The ovaries have reproductive and hormone secretion functions and are crucial throughout the female reproductive lifecycle. Women of childbearing age in China face a serious problem of diminished ovarian reserve (DOR), which can lead to infertility, failed in vitro fertilization (IVF) treatments, miscarriage, and other adverse pregnancy outcomes, severely affecting the safety of women and their offspring. For DOR patients who desire to conceive, failure to intervene and treat promptly can result in irreversible losses and impose a significant psychological burden on them. However, there are currently no clear and reliable interventions that can improve ovarian function and enhance fertility in women with DOR. Therefore, exploring new, safe, and patient-acceptable intervention strategies is urgently needed, as it may bring hope and light to women with DOR. Nutrient supplementation, especially vitamin supplementation, has received increasing attention in disease treatment due to its safety, bioavailability, and effectiveness. Previous studies have shown that vitamin C may play an important role in treating diminished ovarian reserve. However, its effects on ovarian function need to be validated in the population. Based on the above research background, this project will conduct a randomized, placebo-controlled, double-blind, multicenter trial. The study subjects will be DOR infertility patients undergoing IVF/ICSI treatment. The intervention group will receive oral vitamin C supplementation at a dosage of 500 mg per dose, twice a day; the control group will receive a placebo with the same dosage and method for at least three months. Patients will be followed up until delivery outcomes, comparing the IVF/ICSI treatment results between the vitamin C supplementation group and the placebo group. The primary endpoint of this clinical trial is the live birth rate of the IVF/ICSI treatment cycle. Secondary endpoints include indicators of improved ovarian reserve function, ovarian aging molecular clocks, IVF-embryo culture indicators, pregnancy rates, pregnancy complications, and neonatal conditions, thereby providing new clues and theoretical basis for clinical treatment plans for DOR patients.

Participants needed: 1,100
Trial details
Age: 20-45Biological sex: FemaleType: InterventionalSponsor: Peking University Third HospitalUpdated: Jun 17, 2025Locations: 6
Eligibility criteria

Infertile women undergoing their 1st or 2nd IVF treatment [+2]

PGT (preimplantation genetic testing) candidates [+15]

Status: Not yet recruiting

Comparison of Two Protocols in Frozen Embryo Transfer

This randomized clinical trial evaluates two different endometrial preparation protocols-hormone replacement therapy (HRT) and natural cycle-for frozen embryo transfer (FET) in infertile women undergoing assisted reproductive technology (ART). The goal is to compare implantation, clinical pregnancy, and ongoing pregnancy outcomes.

Participants needed: 112
Trial details
Age: 18-42Biological sex: FemaleType: InterventionalSponsor: Malihe MahmoudiniaUpdated: Jun 4, 2025
Eligibility criteria

Not listed