Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT01053052

Study of FemVue(TM) Sono Tubal Evaluation System Method Comparison to HSG

A Comparative Study of Methods for Tubal Patency Determination and Uterine Cavity Evaluation: Sonography With the FemVue(TM) Catheter System vs. Hysterosalpingography (HSG)

Status
Withdrawn
Phase
N/A
Study type
Interventional
Enrollment
0 (actual)
Sponsor
Femasys Inc. · Industry
Sex
Female
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

Multi-center prospective comparison of fallopian tubal patency determination and uterine evaluation interventions using legally marketed devices for their intended purposes, and using each subject as their own control.

Detailed description

Study cancelled prior to recruitment.

Conditions

Interventions

TypeNameDescription
DEVICESonography with FemVue, and HSGSono HSG for FDA 510(k) cleared indication for use

Timeline

Start date
2010-01-01
Primary completion
2013-01-01
Completion
2013-01-01
First posted
2010-01-21
Last updated
2017-05-09

Regulatory

Source: ClinicalTrials.gov record NCT01053052. Inclusion in this directory is not an endorsement.