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Treatment of vascular inner ear disease in vascular patients with pentoxifylline: a controlled, randomized trial.

Abstract
The efficacy of Pentoxifylline in vascular inner ear disease (VIED) was studied comparing PXF and placebo in a 4-week study; 40 patients with vascular disease and monolateral loss of hearing, vertigo, dizziness, tinnitus (analyzed with an analogue scale line), and cochlear flow reduction were included. The aims of the study were to study the effects of PXF (1600 mg daily) in VIED considering clinical outcome and cochlear flow. Of the 20 included patients, 19 completed the study. One dropout in the placebo group was due to low compliance. Intention-to-treat analysis indicated an improvement in cochlear flow (p<0.05) and a decrease in score in both groups. The cochlear flow increase was 287.5% in the PXF group vs 168% in the placebo group (119.5% difference; p<0.02). There was a difference in score decrease (44.1% larger) in the PXF group (p<0.05).Between-group analysis favors PXF considering blood flow and symptoms. Results indicate good efficacy and tolerability of PXF in VIED.
AuthorsM R Cesarone, L Incandela, G Belcaro, M T De Sanctis, A N Nicolaides, M Griffin, G Geroulakos, G Ramaswami
JournalAngiology (Angiology) 2002 Jan-Feb Vol. 53 Suppl 1 Pg. S23-6 ISSN: 0003-3197 [Print] United States
PMID11865831 (Publication Type: Clinical Trial, Journal Article, Randomized Controlled Trial)
Chemical References
  • Vasodilator Agents
  • Pentoxifylline
Topics
  • Cochlea (blood supply, drug effects, physiopathology)
  • Double-Blind Method
  • Ear Diseases (drug therapy, physiopathology)
  • Ear, Inner (drug effects, physiopathology)
  • Female
  • Hemorheology (drug effects)
  • Humans
  • Male
  • Middle Aged
  • Patient Compliance
  • Pentoxifylline (therapeutic use)
  • Regional Blood Flow (drug effects, physiology)
  • Time Factors
  • Treatment Outcome
  • Vascular Diseases (drug therapy, physiopathology)
  • Vasodilator Agents (therapeutic use)

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