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Assess Efficacy of Vardenafil 10mg in Erectile Dysfunction Within Intake of 6 Hours

NCT00668018 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 887

Last updated 2014-12-23

No results posted yet for this study

Summary

Assess efficacy of vardenafil within 6 hours after intake

Conditions

Interventions

DRUG

Levitra (Vardenafil, BAY38-9456)

Vardenafil 10mg orally on demand prior to intercourse

Sponsors & Collaborators

Principal Investigators

  • Bayer Study Director · Bayer

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2003-01-31
Primary Completion
2003-10-31
Completion
2003-10-31

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Entities

Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00668018 on ClinicalTrials.gov