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Ovarian PRP Injections for Improved Embryo Quality Using Embryo Quality Score

Ovarian Platelet-Rich Plasma (oPRP) Injections Improvement In IVF Patients Based On Time-Lapse Incubator Culture for Automated Tracking and AI for Embryo Quality Assessment : A Non-Randomized Propsective Self-Controlled Interventional Study

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07020546
Enrollment
180
Registered
2025-06-13
Start date
2025-07-08
Completion date
2026-08-30
Last updated
2025-07-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Embryo Growth Disorder, Infertility, in Vitro Fertilization, Poor Ovarian Reserve

Brief summary

Patients will have ovarian PRP treatments and embryo development will be observed using time-lapse imaging and AI software.

Detailed description

. oPRP Treatment & Second IVF Cycle (Study Cycle) * Following the first IVF cycle, patients will undergo their first oPRP injection: * Timing: 1-2 weeks after the onset of the next menstrual cycle. * Procedure: Under IV sedation, a patient's autologous PRP will be prepared and injected directly into both ovaries under transvaginal ultrasound guidance. * Second IVF Cycle (oPRP Study Cycle) * The same ovarian stimulation protocol will be used for consistency. * A second oPRP injection will be performed on stimulation days 2-5 to enhance folliculogenesis. * Ovulation will be triggered at the same follicular size thresholds, and oocyte retrieval will follow identical protocols. * Fertilization methodology will be identical to the first cycle unless no fertilization is identified in the first cycle. * Embryo Development Analysis: Up to 15 embryos will be cultured in the AI incubator, where time-lapse imaging will track their morphokinetics, and AI-based analysis will assess embryo viability and implantation potential.

Interventions

PROCEDUREOvarian Platelet-rich plasma (PRP) injections

This is a procedure that our patients receive at our clinic. We want to use the AI software to evaluate embryo development before and after treatment to see if there is a difference in embryo quality after PRP treatment within the same patient.

Sponsors

Generation Next Fertility
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

A NON-RANDOMIZED PROSPECTIVE SELF-CONTROLLED INTERVENTIONAL STUDY

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 47 Years
Healthy volunteers
Yes

Inclusion criteria

* No none contraindications to IVF or PRP treatment * Adequate ovarian reserves and AMH level * Willingness to undergo two IVF cycles and oPRP treatment

Exclusion criteria

* Anovulation due to menopause or perimenopause * Any health conditions that are contraindicated for IVF or oPRP treatment

Design outcomes

Primary

MeasureTime frameDescription
Blastocyst formation and embryo quality1 yearThe number of high quality embryos that are created per cycle

Secondary

MeasureTime frameDescription
Live birth rate per transfer2 yearsThe number of live births following embryo transfer

Countries

United States

Contacts

Primary ContactAlicia L Broussard, PhD
a.broussard@generationnextfertility.com3174456958
Backup ContactJesse Hade, MD
j.hade@generationnextfertility.com2126410906

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026