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Study to Compare the Tolerability and Efficacy of Once Daily Vardenafil vs Vardenafil PRN vs Placebo in Men Immediately After Nerve-sparing Prostatectomy for Improving ED

Primary Purpose

Erectile Dysfunction, Sexual Dysfunction, Physiological

Status
Completed
Phase
Phase 3
Locations
International
Study Type
Interventional
Intervention
Levitra (Vardenafil, BAY38-9456)
Levitra (Vardenafil, BAY38-9456)
Placebo
Sponsored by
Bayer
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Erectile Dysfunction

Eligibility Criteria

18 Years - 64 Years (Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

At Screening

  • Males 18-64 years of age
  • Scheduled to undergo bilateral nerve-sparing radical retropubic BNSRRP, as selected according to the investigator's usual clinical practice
  • Surgery scheduled within about 1 month of screening (Visit 1)
  • Expressed an interest in resuming sexual activity as soon as possible after prostatectomy
  • Heterosexual relationship
  • No pre-operative erectile dysfunction:
  • International Index of Erectile Function (IIEF) Erectile Function Domain Score score EF domain =26 at screening without any therapy/devices for improvement of erections
  • No perforation of the prostate capsule by tumor

At Randomization:

Before being randomized subjects must still be meeting all Screening Inclusion Criteria, as well as the following criteria:

  • bilateral nerve-sparing during the retropubic prostatectomy documented on the operating report
  • BNSRRP occurred within approximately 1 month post screening (Visit 1)
  • No perforation of the prostate capsule by tumor:

No positive tumor margins confirmed after surgery: =T2 stage on pathology report from the surgery

Exclusion Criteria:

  • Subjects who are taking nitrates or nitric oxide donors
  • Subjects who are taking the following inhibitors of cytochrome P 450 CYP 3A4: very potent HIV protease inhibitors (ritonavir, indinavir), the anti-mycotic agents itraconazole and ketoconazole (topical forms are allowed) or erythromycin
  • Known hypersensitivity to Vardenafil
  • Presence of significant penile anatomical abnormalities (e.g. penile fibrosis or Peyronie's disease)
  • History of retinitis pigmentosa
  • Unstable angina pectoris
  • History of myocardial infarction, stroke or life-threatening arrhythmia within the prior 6 months
  • Severe chronic or acute liver disease
  • Symptomatic postural hypotension in the past 6 months
  • NYHA Class III or IV heart failure
  • Life expectancy <3 years
  • Clinical diagnosis of significant untreated sleep apnea or working night shifts (e.g. 23:00h to 7:00 h)
  • Anti-androgens use
  • Residual prostate cancer, or requirement for radiotherapy or ADT after surgery

Sites / Locations

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Placebo Comparator

Arm Label

Arm 1

Arm 2

Arm 3

Arm Description

Outcomes

Primary Outcome Measures

Determine whether early, NIGHTLY dosing with vardenafil Significantly improves recovery of erectile function after surgery as compared to placebo, and whether early PRN dosing with vardenafil also improves recovery of function as compared to placebo

Secondary Outcome Measures

Assess whether early dosing of either NIGHTLY or PRN vardenafil over 9 months, followed by 2 months of withdrawal, increases efficacy of subsequent PRN use significantly better than placebo

Full Information

First Posted
June 26, 2007
Last Updated
October 27, 2014
Sponsor
Bayer
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1. Study Identification

Unique Protocol Identification Number
NCT00492635
Brief Title
Study to Compare the Tolerability and Efficacy of Once Daily Vardenafil vs Vardenafil PRN vs Placebo in Men Immediately After Nerve-sparing Prostatectomy for Improving ED
Official Title
A Randomized, Double-blind, Double-dummy, Multicenter Parallel Group Study to Compare the Tolerability and Efficacy of Once Daily Vardenafil Versus Vardenafil PRN Versus Placebo in Men Immediately After Nerve-sparing Prostatectomy for Improving Erectile Function
Study Type
Interventional

2. Study Status

Record Verification Date
October 2014
Overall Recruitment Status
Completed
Study Start Date
December 2004 (undefined)
Primary Completion Date
September 2007 (Actual)
Study Completion Date
September 2007 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Bayer

4. Oversight

5. Study Description

Brief Summary
A study to assess the efficacy of vardenafil, taken as a tablet both nightly or 'as needed' (immediately before intended sexual activity) compared to placebo, to evaluate its tolerability and if it can help in recovery of erections after a nerve sparing radical prostatectomy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Erectile Dysfunction, Sexual Dysfunction, Physiological

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
628 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Arm 1
Arm Type
Experimental
Arm Title
Arm 2
Arm Type
Experimental
Arm Title
Arm 3
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Levitra (Vardenafil, BAY38-9456)
Intervention Description
9 months DAILY dosage (double blind) 2 months single-blind placebo wash-out period (subject only is blinded) 2 months open-label PRN treatment with active medication
Intervention Type
Drug
Intervention Name(s)
Levitra (Vardenafil, BAY38-9456)
Intervention Description
9 months PRN dosage (double blind) 2 months single-blind placebo wash-out period (subject only is blinded) 2 months open-label PRN treatment with active medication
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
9 months placebo (double blind)2 months single-blind placebo wash-out period (subject only is blinded)2 months open-label PRN treatment with active medication
Primary Outcome Measure Information:
Title
Determine whether early, NIGHTLY dosing with vardenafil Significantly improves recovery of erectile function after surgery as compared to placebo, and whether early PRN dosing with vardenafil also improves recovery of function as compared to placebo
Time Frame
9 months
Secondary Outcome Measure Information:
Title
Assess whether early dosing of either NIGHTLY or PRN vardenafil over 9 months, followed by 2 months of withdrawal, increases efficacy of subsequent PRN use significantly better than placebo
Time Frame
13 months

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
64 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: At Screening Males 18-64 years of age Scheduled to undergo bilateral nerve-sparing radical retropubic BNSRRP, as selected according to the investigator's usual clinical practice Surgery scheduled within about 1 month of screening (Visit 1) Expressed an interest in resuming sexual activity as soon as possible after prostatectomy Heterosexual relationship No pre-operative erectile dysfunction: International Index of Erectile Function (IIEF) Erectile Function Domain Score score EF domain =26 at screening without any therapy/devices for improvement of erections No perforation of the prostate capsule by tumor At Randomization: Before being randomized subjects must still be meeting all Screening Inclusion Criteria, as well as the following criteria: bilateral nerve-sparing during the retropubic prostatectomy documented on the operating report BNSRRP occurred within approximately 1 month post screening (Visit 1) No perforation of the prostate capsule by tumor: No positive tumor margins confirmed after surgery: =T2 stage on pathology report from the surgery Exclusion Criteria: Subjects who are taking nitrates or nitric oxide donors Subjects who are taking the following inhibitors of cytochrome P 450 CYP 3A4: very potent HIV protease inhibitors (ritonavir, indinavir), the anti-mycotic agents itraconazole and ketoconazole (topical forms are allowed) or erythromycin Known hypersensitivity to Vardenafil Presence of significant penile anatomical abnormalities (e.g. penile fibrosis or Peyronie's disease) History of retinitis pigmentosa Unstable angina pectoris History of myocardial infarction, stroke or life-threatening arrhythmia within the prior 6 months Severe chronic or acute liver disease Symptomatic postural hypotension in the past 6 months NYHA Class III or IV heart failure Life expectancy <3 years Clinical diagnosis of significant untreated sleep apnea or working night shifts (e.g. 23:00h to 7:00 h) Anti-androgens use Residual prostate cancer, or requirement for radiotherapy or ADT after surgery
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bayer Study Director
Organizational Affiliation
Bayer
Official's Role
Study Director
Facility Information:
City
Laguna Hills
State/Province
California
ZIP/Postal Code
92653
Country
United States
City
Jeffersonville
State/Province
Indiana
ZIP/Postal Code
47130
Country
United States
City
Des Moines
State/Province
Iowa
ZIP/Postal Code
50309
Country
United States
City
Jackson
State/Province
Mississippi
ZIP/Postal Code
39202
Country
United States
City
Poughkeepsie
State/Province
New York
ZIP/Postal Code
12601
Country
United States
City
Cincinnati
State/Province
Ohio
ZIP/Postal Code
45212-2787
Country
United States
City
Columbus
State/Province
Ohio
ZIP/Postal Code
43214-1419
Country
United States
City
Oklahoma City
State/Province
Oklahoma
ZIP/Postal Code
73104
Country
United States
City
Lancaster
State/Province
Pennsylvania
ZIP/Postal Code
17604
Country
United States
City
Providence
State/Province
Rhode Island
ZIP/Postal Code
02904
Country
United States
City
Spokane
State/Province
Washington
ZIP/Postal Code
99202
Country
United States
City
Graz
State/Province
Steiermark
ZIP/Postal Code
8036
Country
Austria
City
Salzburg
ZIP/Postal Code
5020
Country
Austria
City
Bruxelles - Brussel
ZIP/Postal Code
1000
Country
Belgium
City
Bruxelles - Brussel
ZIP/Postal Code
1200
Country
Belgium
City
Edegem
ZIP/Postal Code
2650
Country
Belgium
City
Hasselt
ZIP/Postal Code
3500
Country
Belgium
City
Leuven
ZIP/Postal Code
3000
Country
Belgium
City
Liege
ZIP/Postal Code
4000
Country
Belgium
City
Calgary
State/Province
Alberta
ZIP/Postal Code
T2V 4R6
Country
Canada
City
Edmonton
State/Province
Alberta
ZIP/Postal Code
T6G 2C8
Country
Canada
City
Barrie
State/Province
Ontario
ZIP/Postal Code
L4M 7G1
Country
Canada
City
London
State/Province
Ontario
ZIP/Postal Code
N6A 4V2
Country
Canada
City
Oakville
State/Province
Ontario
ZIP/Postal Code
L6H 3P1
Country
Canada
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M4N 3M5
Country
Canada
City
Chicoutimi
State/Province
Quebec
ZIP/Postal Code
G7H 4A3
Country
Canada
City
Fleurimont
State/Province
Quebec
ZIP/Postal Code
J1H 5N4
Country
Canada
City
St. John
ZIP/Postal Code
E2L 3J8
Country
Canada
City
Victoria
ZIP/Postal Code
V8R 6T9
Country
Canada
City
Oulu
ZIP/Postal Code
90220
Country
Finland
City
Oulu
ZIP/Postal Code
FI-90100
Country
Finland
City
Tampere
ZIP/Postal Code
33100
Country
Finland
City
Carpentras
ZIP/Postal Code
84200
Country
France
City
Lille
ZIP/Postal Code
59037
Country
France
City
Lyon Cedex
ZIP/Postal Code
69437
Country
France
City
Nimes
ZIP/Postal Code
30000
Country
France
City
Saint Genis Laval Cedex
ZIP/Postal Code
69230
Country
France
City
Mannheim
State/Province
Baden-Württemberg
ZIP/Postal Code
68167
Country
Germany
City
Tübingen
State/Province
Baden-Württemberg
ZIP/Postal Code
72076
Country
Germany
City
München
State/Province
Bayern
ZIP/Postal Code
81377
Country
Germany
City
München
State/Province
Bayern
ZIP/Postal Code
81675
Country
Germany
City
Weiden
State/Province
Bayern
ZIP/Postal Code
92637
Country
Germany
City
Offenbach
State/Province
Hessen
ZIP/Postal Code
63069
Country
Germany
City
Braunschweig
State/Province
Niedersachsen
ZIP/Postal Code
38118
Country
Germany
City
Osnabrück
State/Province
Niedersachsen
ZIP/Postal Code
49076
Country
Germany
City
Dortmund
State/Province
Nordrhein-Westfalen
ZIP/Postal Code
44137
Country
Germany
City
Herne
State/Province
Nordrhein-Westfalen
ZIP/Postal Code
44627
Country
Germany
City
Leverkusen
State/Province
Nordrhein-Westfalen
ZIP/Postal Code
51375
Country
Germany
City
Hamburg
ZIP/Postal Code
20246
Country
Germany
City
Bari
ZIP/Postal Code
70124
Country
Italy
City
Firenze
ZIP/Postal Code
50139
Country
Italy
City
Genova
ZIP/Postal Code
16132
Country
Italy
City
Milano
ZIP/Postal Code
20127
Country
Italy
City
Milano
ZIP/Postal Code
20132
Country
Italy
City
Napoli
ZIP/Postal Code
80131
Country
Italy
City
Trieste
ZIP/Postal Code
34149
Country
Italy
City
Leiden
ZIP/Postal Code
2333 ZA
Country
Netherlands
City
Nijmegen
ZIP/Postal Code
6525 GA
Country
Netherlands
City
Rotterdam
ZIP/Postal Code
3015 GD
Country
Netherlands
City
Moelv
ZIP/Postal Code
2390
Country
Norway
City
Tønsberg
ZIP/Postal Code
3103
Country
Norway
City
Johannesburg
State/Province
Gauteng
ZIP/Postal Code
2193
Country
South Africa
City
Pretoria
State/Province
Gauteng
ZIP/Postal Code
0083
Country
South Africa
City
Pietermaritzburg
State/Province
Kwazulu-Natal
ZIP/Postal Code
3200
Country
South Africa
City
Cape Town
State/Province
Western Cape
ZIP/Postal Code
7505
Country
South Africa
City
Cape Town
State/Province
Western Cape
ZIP/Postal Code
8001
Country
South Africa
City
Vigo
State/Province
Pontevedra
ZIP/Postal Code
36211
Country
Spain
City
Barcelona
ZIP/Postal Code
08025
Country
Spain
City
Barcelona
ZIP/Postal Code
08036
Country
Spain
City
Madrid
ZIP/Postal Code
28046
Country
Spain
City
Málaga
ZIP/Postal Code
29010
Country
Spain
City
Valencia
ZIP/Postal Code
46009
Country
Spain
City
Valencia
ZIP/Postal Code
46026
Country
Spain
City
Göteborg
ZIP/Postal Code
413 45
Country
Sweden
City
Göteborg
ZIP/Postal Code
417 17
Country
Sweden
City
Halmstad
ZIP/Postal Code
301 85
Country
Sweden
City
Lund
ZIP/Postal Code
221 85
Country
Sweden
City
Skövde
ZIP/Postal Code
541 30
Country
Sweden
City
Västerås
ZIP/Postal Code
721 89
Country
Sweden
City
Bern
ZIP/Postal Code
3010
Country
Switzerland
City
Bath
State/Province
Avon
ZIP/Postal Code
BA1 3NG
Country
United Kingdom
City
Bristol
State/Province
Avon
ZIP/Postal Code
BS10 5NB
Country
United Kingdom
City
Slough
State/Province
Berkshire
ZIP/Postal Code
SL2 4HL
Country
United Kingdom
City
Taunton
State/Province
Somerset
ZIP/Postal Code
TA1 5DA
Country
United Kingdom
City
London
ZIP/Postal Code
W6 8RF
Country
United Kingdom
City
Manchester
ZIP/Postal Code
M20 4BX
Country
United Kingdom

12. IPD Sharing Statement

Links:
URL
http://www.clinicaltrialsregister.eu
Description
Click here and search for information of Bayer products for Europe

Learn more about this trial

Study to Compare the Tolerability and Efficacy of Once Daily Vardenafil vs Vardenafil PRN vs Placebo in Men Immediately After Nerve-sparing Prostatectomy for Improving ED

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