Viewing Study NCT06518928



Ignite Creation Date: 2024-10-26 @ 3:35 PM
Last Modification Date: 2024-10-26 @ 3:35 PM
Study NCT ID: NCT06518928
Status: RECRUITING
Last Update Posted: None
First Post: 2024-07-19

Brief Title: SprmPik AI Sperm Selection Study SiD an Assistant for Sperm Selection During Intracytoplasmic Sperm Injection in Medically Assisted Reproduction Effect on Fertilization Blastocyst Formation Early Pregnancy Loss and Consistent Practice A Prospective Pilot Study
Sponsor: None
Organization: None

Study Overview

Official Title: SprmPik AI Assisted Sperm Selection Study an Assistant for Sperm Selection During ICSI
Status: RECRUITING
Status Verified Date: 2024-07
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: SprmPik
Brief Summary: SprmPik AI Assisted Sperm Selection Study SiD an assistant for sperm selection during intracytoplasmic sperm injection in medically assisted reproduction effect on fertilization blastocyst formation early pregnancy loss and consistent practice A prospective pilot study
Detailed Description: The purpose of this research is to evaluate the impact of sperm selection for ICSI using the investigational SiD software on performance outcomes such as the rate of fertilization blastocyst development clinical pregnancy success and other intermediate results in a pilot study

SiD is a software designed to identify evaluate and assist in the sperm selection process within a semen sample according to motility for instance velocity linearity straightness patterns and the shape of the sperm SID uses a mathematical model Its purpose is to assist clinical embryologists in selecting sperm to inject during ICSI Currently embryologists identify and select sperm based on the sperm motility and shape not using any mathematical interphase assistant

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None