Study Design: 15 couples enrolled in the study. Non-blinded and non-randomized, single-center comparison study comparing The Stork® to natural intercourse, using the subjects as their own control/baseline. Subjects used both the Stork kit for conception and the natural intercourse method to evaluate concentrations of sperm in the cervical mucus.
Study Author and Location: Dr. Michael J. Pelekanos, Vice Chairman, Department of Obstetrics and Gynecology, Forbes Regional Hospital in Monroeville, PA.
Time Period: Study was performed over a 10-month time period (November 2014-August 2015).
This Postcoital Sperm Assessment Study is peer-reviewed and published in the Surgical Technology International, Issue XXII, December 2015.