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Completed Phase 3 Interventional

Depression Related Improvement With Vardenafil for Erectile Response

ClinicalTrials.gov ID: NCT00661219

Public ClinicalTrials.gov record NCT00661219. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 22, 2026, 5:12 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized Double-blind Multi-center Parallel Group Three Month Study to Compare the Tolerability and Efficacy of Flexible Dose Vardenafil Versus Placebo in Men With Depression and Erectile Dysfunction.

Study identification

NCT ID
NCT00661219
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Bayer
Industry
Enrollment
280 participants

Conditions and interventions

Interventions

  • Levitra (Vardenafil, BAY38-9456) Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
Male
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 30, 2002
Primary completion
Oct 31, 2003
Completion
Oct 31, 2003
Last update posted
Dec 22, 2014

2002 – 2003

United States locations

U.S. sites
15
U.S. states
11
U.S. cities
14
Facility City State ZIP Site status
Not listed Huntsville Alabama 35801
Not listed Anchorage Alaska 99508
Not listed Beverly Hills California 90212
Not listed Irvine California 92618-3603
Not listed La Mesa California 91942-3058
Not listed San Diego California 92101
Not listed Aventura Florida 33180
Not listed Atlanta Georgia 30308
Not listed Atlanta Georgia 30339
Not listed Boston Massachusetts 02118
Not listed New Brunswick New Jersey 08901
Not listed Albuquerque New Mexico 87131
Not listed New York New York 10032
Not listed Durham North Carolina 27710
Not listed Charlottesville Virginia 22908

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 37 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00661219, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 22, 2014 · Synced Jul 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00661219 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →