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Sperm Preparation Prior to Intrauterine Insemination Study — PIoUS  

Infertility Clinical Trial

Official title:
The Sperm Preparation Prior to Intrauterine Insemination Study (PIoUS)

Clinical Trial Summary

This is a randomized controlled trial comparing density gradient centrifugation and microfluidic sperm sorting in patients undergoing intrauterine insemination to evaluate cumulative pregnancy outcomes.

Clinical Trial Description

Study participants will be randomized to either standard sperm preparation (density gradient centrifugation) versus sperm preparation with the Zymot Multi sperm preparation device for their three month intrauterine insemination treatment course. Patients will follow standard treatment plans designed by their fertility physician and will be followed until referred for prenatal care at 8-10 weeks of pregnancy to determine pregnancy outcomes. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05693220
Study type Interventional
Source University of California, San Francisco
Contact Alisha T Tolani, MD
Phone 6282867307
Email alisha.tolani@ucsf.edu
Status Recruiting
Phase N/A
Start date February 5, 2023
Completion date December 31, 2025
View Details
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