Vardenafil improves urodynamic parameters in men with spinal cord injury: results from a single dose, pilot study

J Urol. 2007 Nov;178(5):2040-3; discussion 2044. doi: 10.1016/j.juro.2007.07.048. Epub 2007 Sep 17.

Abstract

Purpose: We assessed urodynamic changes after vardenafil administration in spinal cord injured male patients on oxybutynin treatment.

Materials and methods: We performed a single center, randomized, double-blind, placebo controlled trial in 25 patients with spinal cord injury who had erectile dysfunction and micturition disorders. A baseline urodynamic test was performed as well as a second urodynamic test 1 to 3 hours after the administration of 20 mg vardenafil and placebo in 15 and 10 cases, respectively. In all patients standard oral oxybutynin administration was not discontinued. Statistical assessment included the 3 urodynamic parameters maximum detrusor pressure during voiding, maximum cystometric capacity and detrusor overactivity volume.

Results: Placebo administration did not affect urodynamic parameters. After vardenafil administration maximum detrusor pressure was significantly decreased (59.3 vs 52.1 cm H(2)O, p <0.001) and maximum cystometric capacity considerably improved (233.5 vs 272 ml, p <0.001). The most dramatic variations were observed for detrusor overactivity volume (174 vs 218 ml, p <0.0001). In 7 patients with American Spinal Injury Association classification A and spinal cord injury above T6 we observed the most significant improvement in the evaluated urodynamic items, including maximum detrusor pressure 57 vs 52 cm H(2)O (p = 0.039), maximum cystometric capacity 253 vs 296 ml (p = 0.004) and detrusor overactivity volume 177 vs 229 ml (p = 0.003).

Conclusions: This trial demonstrates that in spinal cord injured patients a single 20 mg vardenafil administration achieved a significant decrease in maximum detrusor pressure, an improvement in maximum cystometric capacity and a remarkable increase in detrusor overactivity volume value.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Administration, Oral
  • Adult
  • Dose-Response Relationship, Drug
  • Double-Blind Method
  • Erectile Dysfunction / drug therapy
  • Erectile Dysfunction / etiology
  • Erectile Dysfunction / physiopathology*
  • Follow-Up Studies
  • Humans
  • Imidazoles / administration & dosage*
  • Male
  • Mandelic Acids / administration & dosage
  • Middle Aged
  • Parasympatholytics / administration & dosage
  • Phosphodiesterase Inhibitors / administration & dosage*
  • Pilot Projects
  • Piperazines / administration & dosage*
  • Retrospective Studies
  • Spinal Cord Injuries / drug therapy*
  • Spinal Cord Injuries / physiopathology
  • Sulfones / administration & dosage
  • Treatment Outcome
  • Triazines / administration & dosage
  • Urination Disorders / drug therapy
  • Urination Disorders / etiology
  • Urination Disorders / physiopathology*
  • Urodynamics / drug effects*
  • Vardenafil Dihydrochloride

Substances

  • Imidazoles
  • Mandelic Acids
  • Parasympatholytics
  • Phosphodiesterase Inhibitors
  • Piperazines
  • Sulfones
  • Triazines
  • Vardenafil Dihydrochloride
  • oxybutynin