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📊 Resource Allocation by Research Phase:
📚 Data Analysis
🧪 Experimental Design
🔬 Clinical Trials
💊 Treatment Development
This is an exploratory clinical study to presume the optimum usage and dosa...
Status
Completed
Location
Department of Urology, Pusan National University Hospital
Start Date
2008-02
Trial ID
NCT02477436
The aim of this trial is to evaluate the efficacy of type-5 phosphodiestera...
Status
Withdrawn
Location
Ping-Hung Kuo
Start Date
2002-11
Trial ID
NCT00155714
Treatments Being Tested
The aim of this multi-centre, double blind, randomised, controlled trial (D...
Status
Completed
Location
The George Institute for Global Health
Start Date
2014-06
Trial ID
NCT02261727
Treatments Being Tested
This is a phase 2, multi-center, randomized, placebo-controlled, double-bli...
Status
Terminated
Location
The First Affiliated Hospital of Bengbu Medical College
Start Date
2020-11-30
Trial ID
NCT04609397
The goal of this trial is that using tadalafil plus low-intensity extracorp...
Status
Unknown
Location
SBPSU
Start Date
2023-02-01
Trial ID
NCT05823506
Treatments Being Tested
Study H6D-MC-LVHQ is an observational, non-interventional, multi-center, pr...
Status
Completed
Location
University of Alabama Birmingham
Start Date
2010-05
Trial ID
NCT01131104
Treatments Being Tested
The enhancement of cGMP levels at the wound site has shown beneficial effec...
Status
Completed
Location
Deraya university, physiotherapy clinics
Start Date
2025-09-01
Trial ID
NCT07690566
Treatments Being Tested
The purpose of this study is to assess the safety of lodenafil carbonate in...
Status
Withdrawn
Location
Irmandade da Santa Casa de Misericórdia de São Paulo
Start Date
2008-11
Trial ID
NCT00817830
Treatments Being Tested
This is a phase 3, multi-center, randomized, placebo-controlled, double-bli...
Status
Recruiting
Location
Beijing Friendship hospital capital medical hospital
Start Date
2023-11-13
Trial ID
NCT06145893
The purpose of this study is to evaluate the safety and efficacy of tadalaf...
Status
Completed
Location
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Start Date
2009-03
Trial ID
NCT00848081