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| Sponsor: | Bayer |
|---|---|
| Information provided by: | Bayer |
| ClinicalTrials.gov Identifier: | NCT00661700 |
Purpose
To find out more information on how treating impotence with vardenafil in comparison to placebo affects the quality of life (QoL) of men and their partners. Subjects will receive 10mg vardenafil or placebo for 4 weeks followed by an 8 week period when the dose of vardenafil may be reduced to 5mg or increased to 20mg. Subjects will then receive their 'preferred' dose for 14 weeks. During this time Quality of Life Measures will be collected via questionnaires
| Condition | Intervention | Phase |
|---|---|---|
|
Erectile Dysfunction |
Drug: Levitra (Vardenafil, BAY38-9456) Drug: Placebo |
Phase III |
| Study Type: | Interventional |
| Study Design: | Treatment, Randomized, Double Blind (Subject, Investigator), Active Control, Parallel Assignment, Safety/Efficacy Study |
| Official Title: | A Double-Blind "Preferred" Vardenafil Dose Study of QoL and Functional Outcomes in Males With Erectile Dysfunction |
| Enrollment: | 600 |
| Study Start Date: | April 2003 |
| Study Completion Date: | May 2004 |
| Arms | Assigned Interventions |
|---|---|
| Arm 2: Placebo Comparator |
Drug: Placebo
10mg placebo for 4 weeks followed by an 8 week titration period when subjects may be titrated up to 20mg placebo or down to 5mg placebo followed by 14 weeks placebo at preferred dose
|
| Arm 1: Experimental |
Drug: Levitra (Vardenafil, BAY38-9456)
10mg Vardenafil for 4 weeks followed by an 8 week titration period when subjects may be titrated up to 20mg Vardenafil or down to 5mg Vardenafil followed by 14 weeks treatment at preferred dose.
|
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Male |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations
Hide Study Locations| Ireland | |
| Dublin, Ireland, 24 | |
| United Kingdom | |
| Dublin, United Kingdom, 24 | |
| United Kingdom, Berkshire | |
| Reading, Berkshire, United Kingdom, RG7 3SG | |
| United Kingdom, County Durham | |
| Durham, County Durham, United Kingdom, DH1 2QW | |
| United Kingdom, Denbighshire | |
| Rhyl, Denbighshire, United Kingdom, LL18 5UJ | |
| United Kingdom, Devon | |
| Plymouth, Devon, United Kingdom, PL4 8QU | |
| United Kingdom, Greater London | |
| London, Greater London, United Kingdom, NW9 9NH | |
| United Kingdom, Greater Manchester | |
| Manchester, Greater Manchester, United Kingdom, M13 9WL | |
| Manchester, Greater Manchester, United Kingdom, M31 OUH | |
| United Kingdom, Hampshire | |
| Portsmouth, Hampshire, United Kingdom, PO3 6AD | |
| United Kingdom, Middlesex | |
| Northwood, Middlesex, United Kingdom, HA6 2RN | |
| United Kingdom, Norfolk | |
| Norwich, Norfolk, United Kingdom, NR1 3SR | |
| United Kingdom, Northern Ireland | |
| Belfast, Northern Ireland, United Kingdom, BT12 6BA | |
| United Kingdom, Oxfordshire | |
| Chipping Norton, Oxfordshire, United Kingdom, OX7 5AL | |
| United Kingdom, Shropshire | |
| Shrewsbury, Shropshire, United Kingdom, SY1 1RL | |
| United Kingdom, South Glamorgan | |
| Cardiff, South Glamorgan, United Kingdom, CF2 5HW | |
| United Kingdom, South Yorkshire | |
| Doncaster, South Yorkshire, United Kingdom, DN1 2ET | |
| United Kingdom, Staffordshire | |
| Lichfield, Staffordshire, United Kingdom, WS14 9JL | |
| United Kingdom, Strathclyde | |
| Glasgow, Strathclyde, United Kingdom, G21 3UW | |
| Hamilton, Strathclyde, United Kingdom, ML3 ODR | |
| Motherwell, Strathclyde, United Kingdom, ML1 3JX | |
| United Kingdom, Warwickshire | |
| Coventry, Warwickshire, United Kingdom, CV6 4DD | |
| United Kingdom, West Yorkshire | |
| Leeds, West Yorkshire, United Kingdom, LS1 3EX | |
| Study Director: | Bayer Study Director | Bayer |
More Information
| Responsible Party: | Bayer HealthCare AG ( Therapeutic Area Head ) |
| Study ID Numbers: | 10940, CTX0010/0267/A |
| Study First Received: | April 15, 2008 |
| Last Updated: | June 19, 2009 |
| ClinicalTrials.gov Identifier: | NCT00661700 History of Changes |
| Health Authority: | United Kingdom: Medicines and Healthcare Products Regulatory Agency |
|
Erectile Dysfunction Quality of Life |
|
Sexual Dysfunctions, Psychological Phosphodiesterase Inhibitors Vardenafil Sexual Dysfunction, Physiological Molecular Mechanisms of Pharmacological Action Mental Disorders |
Enzyme Inhibitors Genital Diseases, Male Sexual and Gender Disorders Erectile Dysfunction Pharmacologic Actions |