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NCT06629766 · ClinicalTrials.gov registry record · NA

The EPIC Study: Exploring Paternal Age and the Influence on Blastocyst Culture

A NA study of Infertility (IVF Patients) and Sperm DNA Fragmentation, sponsored by Reproductive Medicine Associates of New Jersey.

Recruiting
Registry status
NA
Development phase
100
Enrollment target
1
Study location

NCT06629766 is a NA study of Infertility (IVF Patients) and Sperm DNA Fragmentation that is actively recruiting participants, run by Reproductive Medicine Associates of New Jersey. The registered enrollment target is 100 participants, below the 468-participant average among 9 other Infertility (IVF Patients) trials with a reported enrollment target (79% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT06629766, a NA study of Infertility (IVF Patients) and Sperm DNA Fragmentation, is actively recruiting participants, sponsored by Reproductive Medicine Associates of New Jersey.

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

Study Summary

This study aims to assess the effect of age of the male partner and the reproductive ability of sperm prepared via sperm selection devices (Zymot) compared to routine embryologist selected sperm after density gradient centrifugation (DGC) preparation for intracytoplasmic sperm injection (ICSI) in patients undergoing in vitro fertilization treatment (IVF) of their infertility.

Interventions

  • DEVICE Microfluidic sperm separation device
  • OTHER Density grade centrifugation

Study Locations (1)

New Jersey

  • Reproductive Medicine Associates of New Jersey - Basking Ridge

Trial Details

FieldValue
Enrollment Target 100 participants
Start Date 2025-04-09
Est. Completion 2026-12
Phase NA

What the Registry Record Tells You About NCT06629766

The ClinicalTrials.gov registry entry for NCT06629766 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 468-participant average among 9 other Infertility (IVF Patients) trials with a reported enrollment target (79% lower). The listed sponsor is Reproductive Medicine Associates of New Jersey, which has 51 total studies on file at ClinicalTrials.gov.

The record links to 5 conditions, with Infertility (IVF Patients) appearing as the primary indexed condition, and to 2 interventions - of which Microfluidic sperm separation device is the first listed.

NCT06629766 reports 1 study location spanning 1 distinct geographic area - top geographies include New Jersey.

Frequently Asked Questions

What is clinical trial NCT06629766 about?

NCT06629766 is a clinical study titled "The EPIC Study: Exploring Paternal Age and the Influence on Blastocyst Culture". This study aims to assess the effect of age of the male partner and the reproductive ability of sperm prepared via sperm selection devices (Zymot) compared to routine embryologist selected sperm after density gradient centrifugation (DGC) preparation for intracytoplasmic sperm injection (ICSI) in pa...

What is the current status of trial NCT06629766?

This trial is currently recruiting. It is a NA study. The enrollment target is 100 participants. The study started on 2025-04-09. Estimated completion is 2026-12.

What conditions does trial NCT06629766 study?

This clinical trial studies the following conditions: Infertility (IVF Patients), Sperm DNA Fragmentation, Oocyte Competence, Paternal Age, Sperm Selection.

What interventions are being tested in trial NCT06629766?

The interventions under investigation include: Microfluidic sperm separation device (DEVICE), Density grade centrifugation (OTHER).

Who is sponsoring clinical trial NCT06629766?

This trial is sponsored by Reproductive Medicine Associates of New Jersey, which has 51 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06629766 being conducted?

This trial has 1 study location across New Jersey. 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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