Viewing Study NCT00909233


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Study NCT ID: NCT00909233
Status: COMPLETED
Last Update Posted: 2014-12-15
First Post: 2009-05-08
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: LEVITRA® 20mg Special Drug Use Investigation (Long-term)
Sponsor: Bayer
Organization:

Study Overview

Official Title: LEVITRA® 20mg Special Drug Use Investigation (Long-term)
Status: COMPLETED
Status Verified Date: 2014-12
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: This investigation targets either the patients of 18 years-old or older and under 65 years-old with organic or mixed erectile dysfunction (ED) who cannot obtain sufficient efficacy by dose 10mg of Levitra, and the target patients dose is increased to Levitra 20mg. This investigation will be limited to the patients whose tolerability of Levitra 10mg is judged to be no problem.
Detailed Description: None

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?:

Secondary ID Infos

Secondary ID Type Domain Link View
LV0701JP None None View