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Clinical Trial Summary

To evaluate embryology outcomes after application of a technique known as round spermatid injection (ROSI) into donor oocytes in a high-volume clinical infertility practice.


Clinical Trial Description

The objective of this study is to assess embryology outcomes after implementation of a laboratory protocol known as ROSI at a high-volume clinical infertility practice. All samples from enrolled male patients with azoospermia who proceed with surgical sperm extraction (TESE or microTESE) will be evaluated for the presence of round spermatids. These round spermatids will be used as research samples as opposed to being discarded. The investigators aim to identify whether the injection of round spermatids into donor oocytes can lead to successful fertilization, progression to the blastocyst stage, and euploid status. Performance of ROSI using donor oocytes not intended for implantation will allow the investigators to gain valuable insight regarding fertilization and development without any direct risk to patients or future offspring. These embryos are being generated for research purposes only and will ultimately be destroyed after the study has concluded. The investigators will measure rates of isolation of round spermatids from surgical samples, fertilization rates using donor oocytes, rates of progression to the blastocyst stage, and rates of aneuploidy using the previously described technique of ROSI. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04053309
Study type Observational
Source Reproductive Medicine Associates of New Jersey
Contact
Status Terminated
Phase
Start date August 16, 2019
Completion date January 8, 2021

See also
  Status Clinical Trial Phase
Not yet recruiting NCT06307639 - Seminal Levels of PGK2 and ACRV1 as Predictors of Micro-TESE Results in NOA