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Efficacy and Safety Study of Udenafil to Treat Erectile Dysfunction

NCT01774864 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 349

Last updated 2013-01-24

No results posted yet for this study

Summary

Study Design : multi-center, double-blind, placebo-controlled, randomized,

parallel group, fixed dose design

Phase : Phase III

Conditions

Interventions

DRUG

DA-8159 (Udenafil)

DRUG

Placebo

Sponsors & Collaborators

  • Dong-A Pharmaceutical Co., Ltd.

    lead INDUSTRY

Principal Investigators

  • S W Kim, MD, PhD · the Catholic University of Korea St. Mary's Hospital

  • D G Moon, MD, PhD · Korea University Guro Hospital

  • J J Kim, MD, PhD · Korea University Anam Hospital

  • N C Park, MD, PhD · Pusan National University Hospital

  • S W Lee, MD, PhD · Samsung Medical Center

  • J S Paick, MD, PhD · Seoul National University Hospital

  • T Y Ahn, MD, PhD · Asan Medical Center

  • K H Moon, MD, PhD · Yeungnam University Hospital

  • W S Chung, MD, PhD · Ewha Womans University

  • K S Min, MD, PhD · Inje University

  • J K Park, MD, PhD · Chonbuk National University Hospital

  • D Y Yang, MD, PhD · Kangdong Sacred Heart Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-04-30
Primary Completion
2012-05-31
Completion
2012-05-31

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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 NCT01774864 on ClinicalTrials.gov