check_circleStudy Completed

Erectile Dysfunction, Sexual Dysfunction, Physiological

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

Trial purpose

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.

Key Participants Requirements

Sex

Male

Age

18 - 64 Years
  • 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 , 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
  • - 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

Trial summary

Enrollment Goal
628
Trial Dates
December 2004 - September 2007
Phase
Phase 3
Could I Receive a placebo
Yes
Products
Levitra (Vardenafil, BAY38-9456)
Accepts Healthy Volunteer
No

Where to participate

StatusInstitutionLocation
Completed
Universitätsklinikum Hamburg Eppendorf (UKE)Hamburg, 20246, Germany
Completed
Marienhospital Herne Klinik BörnigHerne, 44627, Germany
Completed
Klinikum Osnabrück GmbHOsnabrück, 49076, Germany
Completed
Klinikum OffenbachOffenbach, 63069, Germany
Completed
Klinikum Leverkusen gGmbHLeverkusen, 51375, Germany
Completed
Southmead HospitalBristol, BS10 5NB, United Kingdom
Completed
Wexham Park HospitalSlough, SL2 4HL, United Kingdom
Completed
Taunton and Somerset HospitalTaunton, TA1 5DA, United Kingdom
Completed
Urological Associates of LancasterLancaster, 17604, United States
Completed
Columbus Urology Research, LLCColumbus, 43214-1419, United States
Completed
Iowa Clinic,PC/ Iowa UrololgyDes Moines, 50309, United States
Completed
Hôpital Claude Huriez - LilleLILLE, 59037, France
Completed
Hôpital Henry Gabrielle - Saint Genis Laval CedexSAINT GENIS LAVAL CEDEX, 69230, France
Completed
Synergia - CarpentrasCARPENTRAS, 84200, France
Completed
IRCCS Fondazione San RaffaeleMilano, 20127, Italy
Completed
Klinikum der Eberhard-Karls-Universität TübingenTübingen, 72076, Germany
Completed
Städtisches Klinikum Braunschweig gGmbHBraunschweig, 38118, Germany
Completed
Kliniken Nordoberpfalz AG - Klinikum WeidenWeiden, 92637, Germany
Completed
Klinikum rechts der IsarMünchen, 81675, Germany
Completed
Klinikum Mannheim gGmbHMannheim, 68167, Germany
Completed
LMU Klinikum der Universität München - GroßhadernMünchen, 81377, Germany
Completed
Klinikum Dortmund gGmbHDortmund, 44137, Germany
Completed
Charing Cross HospitalLondon, W6 8RF, United Kingdom
Completed
Royal United HospitalBath, BA1 3NG, United Kingdom
Completed
Christie HospitalManchester, M20 4BX, United Kingdom
Completed
Metropolitan Urology Associates, PCJeffersonville, 47130, United States
Completed
Hudson Valley Urology CenterPoughkeepsie, 12601, United States
Completed
South Coast Urological Medical GroupLaguna Hills, 92653, United States
Completed
The Urology GroupCincinnati, 45212-2787, United States
Completed
A.O.U. Federico IINapoli, 80131, Italy
Completed
A.O.U. Policlinico ConsorzialeBari, 70124, Italy
Completed
Hospital Universitari i Politècnic La FeValencia, 46026, Spain
Completed
Hospital Regional Carlos HayaMálaga, 29010, Spain
Completed
Hospital Fundació PuigvertBarcelona, 08025, Spain
Completed
St.Joseph's Health Care-LondonLondon, N6A 4V2, Canada
Completed
Edmonton Prostate & Urological CentreEdmonton, T6G 2C8, Canada
Completed
Coburg Street Medical ClinicSt. John, E2L 3J8, Canada
Completed
Cente Hospitalier Universitaire de Sherbrooke-FleurimontFleurimont, J1H 5N4, Canada
Completed
Sunnybrook Health Sciences CentreToronto, M4N 3M5, Canada
Completed
Clinique d'Urologie du SaguenayChicoutimi, G7H 4A3, Canada
Completed
UZ Leuven GasthuisbergLEUVEN, 3000, Belgium
Completed
CU Saint-Luc/UZ St-LucBRUXELLES - BRUSSEL, 1200, Belgium
Completed
Clinique Saint-Jean/Kliniek Sint JanBRUXELLES - BRUSSEL, 1000, Belgium
Completed
Leids Universitair Medisch CentrumLeiden, 2333 ZA, Netherlands
Completed
Mississippi Urology ClinicJackson, 39202, United States
Completed
Office of Dr. Roger Fincher, MDSpokane, 99202, United States
Completed
Oklahoma University Health Science CenterOklahoma City, 73104, United States
Completed
University Urological Research InstituteProvidence, 02904, United States
Completed
Hôpital Edouard Herriot - Lyon CedexLYON CEDEX, 69437, France
Completed
Hopital Carémeau - NîmesNIMES, 30000, France
Completed
IRCCS Fondazione San RaffaeleMilano, 20132, Italy
Completed
A.O.U. Ospedali Riuniti TriesteTrieste, 34149, Italy
Completed
A.O.U. CareggiFirenze, 50139, Italy
Completed
IRCCS A.O.U. San Martino – IST Ist. Nazionale Ricerca CancroGenova, 16132, Italy
Completed
A.O.U. CareggiFirenze, 50139, Italy
Completed
Hospital Clínic i Provincial de BarcelonaBarcelona, 08036, Spain
Completed
Hospital Universitario "La Paz"Madrid, 28046, Spain
Completed
Instituto Valenciano de OncologíaValencia, 46009, Spain
Completed
Hospital Policlínico de Vigo - Clínica PovisaVigo, 36211, Spain
Completed
The Male Health CentresOakville, L6H 3P1, Canada
Completed
Erasmus Medisch CentrumROTTERDAM, 3015 GD, Netherlands
Completed
Sahlgrenska UniversitetssjukhusetGöteborg, 413 45, Sweden
Completed
Skånes UniversitetssjukhusLund, 221 85, Sweden
Completed
Lundby Sjukhus ABGöteborg, 417 17, Sweden
Completed
Moelv SpesialistsenterMoelv, 2390, Norway
Completed
Sykehuset i Vestfold HF, TønsbergTønsberg, 3103, Norway
Completed
Pretoria Urology HospitalPRETORIA, 0083, South Africa
Completed
Cape Town Medi-ClinicCape Town, 8001, South Africa
Completed
Landeskrankenhaus SalzburgSalzburg, 5020, Austria
Completed
Medizinische Universität GrazGraz, 8036, Austria
Completed
Suomen Terveystalo Oyj / Gynekologi- ja UrologikeskusTampere, 33100, Finland
Completed
Terveystalo OuluOulu, FI-90100, Finland
Completed
Oulun yliopistollinen sairaalaOulu, 90220, Finland
Completed
Prostate Cancer InstituteCalgary, T2V 4R6, Canada
Completed
CAN-MED Clinical Research, IncVictoria, V8R 6T9, Canada
Completed
Male/Female Health & Research CentreBarrie, L4M 7G1, Canada
Completed
CHU de LiègeLIEGE, 4000, Belgium
Completed
Dr Van RenterghemHASSELT, 3500, Belgium
Completed
UZ AntwerpenEDEGEM, 2650, Belgium
Completed
Universitair Medisch Centrum St. RadboudNIJMEGEN, 6525 GA, Netherlands
Completed
LänssjukhusetHalmstad, 301 85, Sweden
Completed
ED-KlinikenSkövde, 541 30, Sweden
Completed
CentrallasarettetVästerås, 721 89, Sweden
Completed
University of WitwatersrandJohannesburg, 2193, South Africa
Completed
University of StellenboschCape Town, 7505, South Africa
Completed
St Annes Hospital Medical CentrePietermaritzburg, 3200, South Africa
Completed
Inselspital BernBern, 3010, Switzerland

Primary Outcome

  • 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
    date_rangeTime Frame:
    9 months
    enhanced_encryption
    Safety Issue:
    no

Secondary Outcome

  • 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
    date_rangeTime Frame:
    13 months
    enhanced_encryption
    Safety Issue:
    no

Trial design

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
Trial Type
Interventional
Intervention Type
Drug
Trial Purpose
Treatment
Allocation
Randomized
Blinding
Double Blind
Assignment
Parallel Assignment
Trial Arms
3