At a glance
ClinicalIndex Comparison RecordN/ACompleted· 22 enrolled
Drug / intervention
Evie Slow-release Insemination Device +1 moredevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Patient Satisfaction and Tolerability With the Evie® Slow-Release Insemination Device: Pilot Study
In Brief
A clinical study evaluating Evie Slow-release Insemination Device and Traditional Intrauterine Insemination for Infertility. Completed, enrolled 22 participants across 1 site.
Detailed Summary
The purpose of this study is to determine patient satisfaction and tolerability of the Evie® slow-release insemination device for US population. Additionally, to assess cramping with the device and to determine pregnancy rates using the slow insemination device compared to standard IUI.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsInfertility
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedOct 2013
Enrollment StartJan 2014
Primary CompletionMar 2015
TodayJul 2026
First PostedOct 25, 2013
Enrollment StartJan 1, 2014
Primary CompletionMar 1, 2015
TodayJul 2, 2026
Enrollment to primary: 1.2 yearsPosted 12.7 years ago
Interventions
Evie Slow-release Insemination Devicedevice
Traditional Intrauterine Inseminationother