CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 48 enrolled
Drug / intervention
delivery systemother
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.

Search/NCT01008605
NCT01008605Phase 3Completed

Representative Users Study Of Operating Characteristics Of The Caverject Delivery System.

Pfizer·interventional·Posted Nov 6, 2009·Updated Apr 6, 2012

In Brief

A Phase 3 clinical trial evaluating delivery system for Erectile Dysfunction. Completed, enrolled 48 participants across 2 sites.

Detailed Summary

The purpose of this study is to demonstrate the usability of the system.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 3CompletedFinished
20102011201220132014201520162017201820192020202120222023202420252026
First PostedNov 6, 2009
Enrollment StartFeb 1, 2011
Primary CompletionFeb 1, 2011
TodayJul 2, 2026
Enrollment to primary: 0 daysPosted 16.7 years ago

Interventions

delivery systemother

syringe