Viewing Study NCT01008605


Ignite Creation Date: 2025-12-25 @ 3:19 AM
Ignite Modification Date: 2025-12-26 @ 1:57 AM
Study NCT ID: NCT01008605
Status: COMPLETED
Last Update Posted: 2012-04-06
First Post: 2009-11-05
Is NOT Gene Therapy: False
Has Adverse Events: True

Brief Title: Caverject User Study
Sponsor: Pfizer
Organization:

Study Overview

Official Title: Representative Users Study Of Operating Characteristics Of The Caverject Delivery System.
Status: COMPLETED
Status Verified Date: 2012-04
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this study is to demonstrate the usability of the system.
Detailed Description: demonstrate usability

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: