WHO ICTRP trial
A randomized, explorative, double-blind, double-dummy, multi-center, parallel…
EUCTR2005-001678-28-DE · EU Clinical Trials Register · Not Recruiting
Key facts
| Trial ID | EUCTR2005-001678-28-DE |
|---|---|
| Public title | A randomized, explorative, double-blind, double-dummy, multi-center, parallel group study to assess sustainable efficacy of once daily vardenafil (10 mg) for 12 and 24 weeks versus vardenafil PRN in men with mild or mild to moderate erectile dysfunction - RESTORE |
| Scientific title | A randomized, explorative, double-blind, double-dummy, multi-center, parallel group study to assess sustainable efficacy of once daily vardenafil (10 mg) for 12 and 24 weeks versus vardenafil PRN in men with mild or mild to moderate erectile dysfunction - RESTORE |
| Primary sponsor | Bayer Healthcare AG |
| Registry | EU Clinical Trials Register |
| Recruitment status | Not Recruiting |
| Study type | Interventional clinical trial of medicinal product |
| Countries | Germany |
| Conditions | Erectile Dysfunction Classification code 10061461 |
| Interventions | Trade Name: Levitra 10 mg Filmtabletten Product Name: Levitra Product Code: Bay 38-9456 Pharmaceutical Form: Film-coated tablet INN or Proposed INN: Vardenafil-HCL CAS Number: 224785-91-5 Current Sponsor code: BAY 38-9456 / SB-782528… |
| Registration date | Feb 8, 2005 |
| Target size | 267 |
| Secondary IDs | BAY 38-9456 / IMPACT 11875 |
| Registry page | clinicaltrialsregister.eu |
At a glance
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About WHO ICTRP trial registrations
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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date: