Effect of Nightly versus On-Demand Vardenafil on Recovery of Erectile Function in Men Following Bilateral Nerve-Sparing Radical Prostatectomy

To date, no data have been available from large, well-designed trials comparing on demand and nightly dosing of phosphodiesterase type 5 (PDE5) inhibitors on recovery of erectile function in postprostatectomy patients with erectile dysfunction (ED). To investigate the effect of early postoperative d...

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Published inEuropean urology Vol. 54; no. 4; pp. 924 - 931
Main Authors Montorsi, Francesco, Brock, Gerald, Lee, Jay, Shapiro, JoAnn, Van Poppel, Hendrik, Graefen, Markus, Stief, Christian
Format Journal Article
LanguageEnglish
Published Oxford Elsevier B.V 01.10.2008
Elsevier
Subjects
Online AccessGet full text
ISSN0302-2838
1873-7560
DOI10.1016/j.eururo.2008.06.083

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Abstract To date, no data have been available from large, well-designed trials comparing on demand and nightly dosing of phosphodiesterase type 5 (PDE5) inhibitors on recovery of erectile function in postprostatectomy patients with erectile dysfunction (ED). To investigate the effect of early postoperative dosing with vardenafil, administered either nightly or on demand, compared with placebo on recovery of erectile function in men with ED following bilateral nerve-sparing radical prostatectomy (NSRP) surgery. A randomised, double-blind, double-dummy, multicentre, parallel group study conducted at 87 centres across Europe, Canada, South Africa, and the United States. For inclusion, patients had to be scheduled to undergo bilateral NSRP within 1 mo of screening and have a normal International Index of Erectile Function erectile function domain (IIEF-EF) score of ≥26 at screening. A total of 628 men, aged 18–64 yr, were randomised to treatment. Study design consisted of a 9-mo double-blind treatment period, a 2-mo single-blind washout period, and an optional 2-mo open-label period. Patients received placebo, nightly vardenafil, or on demand vardenafil. Primary outcome measure was the percentage of subjects with an IIEF-EF score of ≥22 after the 2-mo washout period. Secondary variables included mean per-patient success rates for Sexual Encounter Profile (SEP) questions 2 and 3. No statistically significant differences were observed among treatment groups in the proportion of patients with an IIEF-EF score of ≥22 or in SEP3 success rates after the washout period. On-demand vardenafil treatment resulted in significantly greater IIEF-EF scores and better SEP3 response rates than placebo over the entire treatment period. In this study of men with ED following bilateral NSRP, vardenafil was efficacious when used on demand, supporting a paradigm shift towards on demand dosing with PDE5 inhibitors in this patient group. European clinical trials database (EudraCT; available at http://eudract.emea.europa.eu/). Trial registration number: 11336. This first, large, multicentre study compared nightly vardenafil with on demand use in men with erectile dysfunction following nerve-sparing radical prostatectomy surgery. On demand vardenafil was efficacious in this patient group, and nightly vardenafil use had no effect beyond that of on demand dosing.
AbstractList To date, no data have been available from large, well-designed trials comparing on demand and nightly dosing of phosphodiesterase type 5 (PDE5) inhibitors on recovery of erectile function in postprostatectomy patients with erectile dysfunction (ED). To investigate the effect of early postoperative dosing with vardenafil, administered either nightly or on demand, compared with placebo on recovery of erectile function in men with ED following bilateral nerve-sparing radical prostatectomy (NSRP) surgery. A randomised, double-blind, double-dummy, multicentre, parallel group study conducted at 87 centres across Europe, Canada, South Africa, and the United States. For inclusion, patients had to be scheduled to undergo bilateral NSRP within 1 mo of screening and have a normal International Index of Erectile Function erectile function domain (IIEF-EF) score of ≥26 at screening. A total of 628 men, aged 18–64 yr, were randomised to treatment. Study design consisted of a 9-mo double-blind treatment period, a 2-mo single-blind washout period, and an optional 2-mo open-label period. Patients received placebo, nightly vardenafil, or on demand vardenafil. Primary outcome measure was the percentage of subjects with an IIEF-EF score of ≥22 after the 2-mo washout period. Secondary variables included mean per-patient success rates for Sexual Encounter Profile (SEP) questions 2 and 3. No statistically significant differences were observed among treatment groups in the proportion of patients with an IIEF-EF score of ≥22 or in SEP3 success rates after the washout period. On-demand vardenafil treatment resulted in significantly greater IIEF-EF scores and better SEP3 response rates than placebo over the entire treatment period. In this study of men with ED following bilateral NSRP, vardenafil was efficacious when used on demand, supporting a paradigm shift towards on demand dosing with PDE5 inhibitors in this patient group. European clinical trials database (EudraCT; available at http://eudract.emea.europa.eu/). Trial registration number: 11336. This first, large, multicentre study compared nightly vardenafil with on demand use in men with erectile dysfunction following nerve-sparing radical prostatectomy surgery. On demand vardenafil was efficacious in this patient group, and nightly vardenafil use had no effect beyond that of on demand dosing.
Background: To date, no data have been available from large, well-designed trials comparing on demand and nightly dosing of phosphodiesterase type 5 (PDE5) inhibitors on recovery of erectile function in postprostatectomy patients with erectile dysfunction (ED). Objective To investigate the effect of early postoperative dosing with vardenafil, administered either nightly or on demand, compared with placebo on recovery of erectile function in men with ED following bilateral nerve-sparing radical prostatectomy (NSRP) surgery. Design, setting, and participants A randomised, double-blind, double-dummy, multicentre, parallel group study conducted at 87 centres across Europe, Canada, South Africa, and the United States. For inclusion, patients had to be scheduled to undergo bilateral NSRP within 1 mo of screening and have a normal International Index of Erectile Function erectile function domain (IIEF-EF) score of >=26 at screening. A total of 628 men, aged 18-64 yr, were randomised to treatment. Study design consisted of a 9-mo double-blind treatment period, a 2-mo single-blind washout period, and an optional 2-mo open-label period. Intervention Patients received placebo, nightly vardenafil, or on demand vardenafil. Measurements Primary outcome measure was the percentage of subjects with an IIEF-EF score of >=22 after the 2-mo washout period. Secondary variables included mean per-patient success rates for Sexual Encounter Profile (SEP) questions 2 and 3. Results and limitations No statistically significant differences were observed among treatment groups in the proportion of patients with an IIEF-EF score of >=22 or in SEP3 success rates after the washout period. On-demand vardenafil treatment resulted in significantly greater IIEF-EF scores and better SEP3 response rates than placebo over the entire treatment period. Conclusions In this study of men with ED following bilateral NSRP, vardenafil was efficacious when used on demand, supporting a paradigm shift towards on demand dosing with PDE5 inhibitors in this patient group. Trial registration European clinical trials database (EudraCT; available at http://eudract.emea.europa.eu/). Trial registration number: 11336.
To date, no data have been available from large, well-designed trials comparing on demand and nightly dosing of phosphodiesterase type 5 (PDE5) inhibitors on recovery of erectile function in postprostatectomy patients with erectile dysfunction (ED). To investigate the effect of early postoperative dosing with vardenafil, administered either nightly or on demand, compared with placebo on recovery of erectile function in men with ED following bilateral nerve-sparing radical prostatectomy (NSRP) surgery. A randomised, double-blind, double-dummy, multicentre, parallel group study conducted at 87 centres across Europe, Canada, South Africa, and the United States. For inclusion, patients had to be scheduled to undergo bilateral NSRP within 1 mo of screening and have a normal International Index of Erectile Function erectile function domain (IIEF-EF) score of > or =26 at screening. A total of 628 men, aged 18-64 yr, were randomised to treatment. Study design consisted of a 9-mo double-blind treatment period, a 2-mo single-blind washout period, and an optional 2-mo open-label period. Patients received placebo, nightly vardenafil, or on demand vardenafil. Primary outcome measure was the percentage of subjects with an IIEF-EF score of > or =22 after the 2-mo washout period. Secondary variables included mean per-patient success rates for Sexual Encounter Profile (SEP) questions 2 and 3. No statistically significant differences were observed among treatment groups in the proportion of patients with an IIEF-EF score of > or =22 or in SEP3 success rates after the washout period. On-demand vardenafil treatment resulted in significantly greater IIEF-EF scores and better SEP3 response rates than placebo over the entire treatment period. In this study of men with ED following bilateral NSRP, vardenafil was efficacious when used on demand, supporting a paradigm shift towards on demand dosing with PDE5 inhibitors in this patient group. European clinical trials database (EudraCT; available at http://eudract.emea.europa.eu/). 11336.
To date, no data have been available from large, well-designed trials comparing on demand and nightly dosing of phosphodiesterase type 5 (PDE5) inhibitors on recovery of erectile function in postprostatectomy patients with erectile dysfunction (ED).BACKGROUNDTo date, no data have been available from large, well-designed trials comparing on demand and nightly dosing of phosphodiesterase type 5 (PDE5) inhibitors on recovery of erectile function in postprostatectomy patients with erectile dysfunction (ED).To investigate the effect of early postoperative dosing with vardenafil, administered either nightly or on demand, compared with placebo on recovery of erectile function in men with ED following bilateral nerve-sparing radical prostatectomy (NSRP) surgery.OBJECTIVETo investigate the effect of early postoperative dosing with vardenafil, administered either nightly or on demand, compared with placebo on recovery of erectile function in men with ED following bilateral nerve-sparing radical prostatectomy (NSRP) surgery.A randomised, double-blind, double-dummy, multicentre, parallel group study conducted at 87 centres across Europe, Canada, South Africa, and the United States. For inclusion, patients had to be scheduled to undergo bilateral NSRP within 1 mo of screening and have a normal International Index of Erectile Function erectile function domain (IIEF-EF) score of > or =26 at screening. A total of 628 men, aged 18-64 yr, were randomised to treatment. Study design consisted of a 9-mo double-blind treatment period, a 2-mo single-blind washout period, and an optional 2-mo open-label period.DESIGN, SETTING, AND PARTICIPANTSA randomised, double-blind, double-dummy, multicentre, parallel group study conducted at 87 centres across Europe, Canada, South Africa, and the United States. For inclusion, patients had to be scheduled to undergo bilateral NSRP within 1 mo of screening and have a normal International Index of Erectile Function erectile function domain (IIEF-EF) score of > or =26 at screening. A total of 628 men, aged 18-64 yr, were randomised to treatment. Study design consisted of a 9-mo double-blind treatment period, a 2-mo single-blind washout period, and an optional 2-mo open-label period.Patients received placebo, nightly vardenafil, or on demand vardenafil.INTERVENTIONPatients received placebo, nightly vardenafil, or on demand vardenafil.Primary outcome measure was the percentage of subjects with an IIEF-EF score of > or =22 after the 2-mo washout period. Secondary variables included mean per-patient success rates for Sexual Encounter Profile (SEP) questions 2 and 3.MEASUREMENTSPrimary outcome measure was the percentage of subjects with an IIEF-EF score of > or =22 after the 2-mo washout period. Secondary variables included mean per-patient success rates for Sexual Encounter Profile (SEP) questions 2 and 3.No statistically significant differences were observed among treatment groups in the proportion of patients with an IIEF-EF score of > or =22 or in SEP3 success rates after the washout period. On-demand vardenafil treatment resulted in significantly greater IIEF-EF scores and better SEP3 response rates than placebo over the entire treatment period.RESULTS AND LIMITATIONSNo statistically significant differences were observed among treatment groups in the proportion of patients with an IIEF-EF score of > or =22 or in SEP3 success rates after the washout period. On-demand vardenafil treatment resulted in significantly greater IIEF-EF scores and better SEP3 response rates than placebo over the entire treatment period.In this study of men with ED following bilateral NSRP, vardenafil was efficacious when used on demand, supporting a paradigm shift towards on demand dosing with PDE5 inhibitors in this patient group.CONCLUSIONSIn this study of men with ED following bilateral NSRP, vardenafil was efficacious when used on demand, supporting a paradigm shift towards on demand dosing with PDE5 inhibitors in this patient group.European clinical trials database (EudraCT; available at http://eudract.emea.europa.eu/).TRIAL REGISTRATIONEuropean clinical trials database (EudraCT; available at http://eudract.emea.europa.eu/).11336.TRIAL REGISTRATION NUMBER11336.
Abstract Background To date, no data have been available from large, well-designed trials comparing on demand and nightly dosing of phosphodiesterase type 5 (PDE5) inhibitors on recovery of erectile function in postprostatectomy patients with erectile dysfunction (ED). Objective To investigate the effect of early postoperative dosing with vardenafil, administered either nightly or on demand, compared with placebo on recovery of erectile function in men with ED following bilateral nerve-sparing radical prostatectomy (NSRP) surgery. Design, setting, and participants A randomised, double-blind, double-dummy, multicentre, parallel group study conducted at 87 centres across Europe, Canada, South Africa, and the United States. For inclusion, patients had to be scheduled to undergo bilateral NSRP within 1 mo of screening and have a normal International Index of Erectile Function erectile function domain (IIEF-EF) score of ≥26 at screening. A total of 628 men, aged 18–64 yr, were randomised to treatment. Study design consisted of a 9-mo double-blind treatment period, a 2-mo single-blind washout period, and an optional 2-mo open-label period. Intervention Patients received placebo, nightly vardenafil, or on demand vardenafil. Measurements Primary outcome measure was the percentage of subjects with an IIEF-EF score of ≥22 after the 2-mo washout period. Secondary variables included mean per-patient success rates for Sexual Encounter Profile (SEP) questions 2 and 3. Results and limitations No statistically significant differences were observed among treatment groups in the proportion of patients with an IIEF-EF score of ≥22 or in SEP3 success rates after the washout period. On-demand vardenafil treatment resulted in significantly greater IIEF-EF scores and better SEP3 response rates than placebo over the entire treatment period. Conclusions In this study of men with ED following bilateral NSRP, vardenafil was efficacious when used on demand, supporting a paradigm shift towards on demand dosing with PDE5 inhibitors in this patient group. Trial registration European clinical trials database (EudraCT; available at http://eudract.emea.europa.eu/ ). Trial registration number: 11336.
Author Lee, Jay
Van Poppel, Hendrik
Brock, Gerald
Graefen, Markus
Shapiro, JoAnn
Stief, Christian
Montorsi, Francesco
Author_xml – sequence: 1
  givenname: Francesco
  surname: Montorsi
  fullname: Montorsi, Francesco
  email: montorsi.francesco@hsr.it
  organization: Universita Vita Salute San Raffaele, Milan, Italy
– sequence: 2
  givenname: Gerald
  surname: Brock
  fullname: Brock, Gerald
  organization: University of Western Ontario, London, Ontario, Canada
– sequence: 3
  givenname: Jay
  surname: Lee
  fullname: Lee, Jay
  organization: Rockyview General Hospital, Alberta, Canada
– sequence: 4
  givenname: JoAnn
  surname: Shapiro
  fullname: Shapiro, JoAnn
  organization: Bayer HealthCare Pharmaceuticals Inc., Montville, New Jersey, USA
– sequence: 5
  givenname: Hendrik
  surname: Van Poppel
  fullname: Van Poppel, Hendrik
  organization: Universitair Ziekenhuis Gasthuisberg, Leuven, Belgium
– sequence: 6
  givenname: Markus
  surname: Graefen
  fullname: Graefen, Markus
  organization: Martini Clinic - Prostate Cancer Center, Hamburg, Germany
– sequence: 7
  givenname: Christian
  surname: Stief
  fullname: Stief, Christian
  organization: Department of Urology, Ludwig-Maximilians-University, Munich, Germany
BackLink http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20679279$$DView record in Pascal Francis
https://www.ncbi.nlm.nih.gov/pubmed/18640769$$D View this record in MEDLINE/PubMed
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Issue 4
Keywords Erectile dysfunction
Vardenafil
Phosphodiesterase type-5 inhibitor
Radical prostatectomy
Nephrology
Vasodilator agent
3',5'-Cyclic-GMP phosphodiesterase
Erection
Sexual dysfunction
Bilateral
Male
Esterases
Phosphoric diester hydrolases
Recovery
Urology
Conservative surgery
Adult
Male genital diseases
Demand
Human
3',5'-Cyclic-nucleotide phosphodiesterase
Erection disorders
Enzyme
Enzyme inhibitor
Phosphodiesterase inhibitor
Phosphodiesterase 5 inhibitor
Treatment
Hydrolases
Prostatectomy
Comparative study
Language English
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Snippet To date, no data have been available from large, well-designed trials comparing on demand and nightly dosing of phosphodiesterase type 5 (PDE5) inhibitors on...
Abstract Background To date, no data have been available from large, well-designed trials comparing on demand and nightly dosing of phosphodiesterase type 5...
Background: To date, no data have been available from large, well-designed trials comparing on demand and nightly dosing of phosphodiesterase type 5 (PDE5)...
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SubjectTerms Biological and medical sciences
Double-Blind Method
Erectile dysfunction
Erectile Dysfunction - drug therapy
Erectile Dysfunction - etiology
Humans
Imidazoles - administration & dosage
Male
Medical sciences
Middle Aged
Nephrology. Urinary tract diseases
Phosphodiesterase Inhibitors - administration & dosage
Phosphodiesterase type-5 inhibitor
Piperazines - administration & dosage
Prostate - innervation
Prostatectomy - adverse effects
Prostatectomy - methods
Radical prostatectomy
Recovery of Function
Sulfones - administration & dosage
Triazines - administration & dosage
Urology
Vardenafil
Vardenafil Dihydrochloride
Title Effect of Nightly versus On-Demand Vardenafil on Recovery of Erectile Function in Men Following Bilateral Nerve-Sparing Radical Prostatectomy
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https://www.ncbi.nlm.nih.gov/pubmed/18640769
https://www.proquest.com/docview/19507781
https://www.proquest.com/docview/69524229
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