Pregabalin for the treatment of painful diabetic peripheral neuropathy: a double-blind, placebo-controlled trial

被引:490
作者
Rosenstock, J
Michael, TB
LaMoreaux, L
Sharma, U
机构
[1] Dallas Diabet & Endo Res Ctr, Dallas, TX 75230 USA
[2] Palm Beach Neurol Ctr, Palm Beach Gardens, FL USA
[3] Pfizer Global Res & Dev, Ann Arbor, MI USA
关键词
painful diabetic neuropathy; anticonvulsants; pregabalin;
D O I
10.1016/j.pain.2004.05.001
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
A randomized, double-blind, placebo-controlled, parallel-group, multicenter, 8-week trial (with subsequent open-label phase) evaluated the effectiveness of pregabalin in alleviating pain associated with diabetic peripheral neuropathy (DPN). For enrollment, patients must have had at baseline: 1- to 5-year history of DPN pain; pain score : 40 mm (Short-Form McGill Pain Questionnaire [SF-MPQ] visual analogue scale); average daily pain score of greater than or equal to 4 (11-point numerical pain rating scale [0 = no pain, 10 worst possible pain]). One hundred forty-six (146) patients were randomized to receive placebo (n = 70) or pregabalin 300 mg/day (n 76). Primary efficacy measure was endpoint mean pain score from daily patient diaries (11-point numerical pain rating scale). Secondary measures included SF-MPQ scores; sleep interference scores; Patient and Clinical Global Impression of Change (PGIC and CGIC); Short Form-36 (SF-36) Health Survey scores; and Profile of Mood States (POMS) scores. Safety assessment included incidence and intensity of adverse events, physical and neurological examinations, and laboratory evaluations. Pregabalin produced significant improvements versus placebo for mean pain scores (P < 0.0001); mean sleep interference scores (P < 0.0001); total SF-MPQ score (P < 0.01); SF-36 Bodily Pain subscale (P < 0.03); PGIC (P = 0.001); and Total Mood Disturbance and Tension-Anxiety components of POMS (P < 0.03). Pain relief and improved sleep began during week I and remained significant throughout the study (P < 0.01). Pregabalin was well tolerated despite a greater incidence of dizziness and somnolence than placebo. Most adverse events were mild to moderate and did not result in withdrawal. Pregabalin was safe and effective in decreasing pain associated with DPN, and also improved mood, sleep disturbance, and quality of life. (C) 2004 International Association for the Study of Pain. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:628 / 638
页数:11
相关论文
共 45 条
[1]  
*AM DIAB ASS, 2004, ALL DIAB
[2]  
[Anonymous], SAS STAT US GUID VER
[3]   THE NATURAL-HISTORY OF ACUTE PAINFUL NEUROPATHY IN DIABETES-MELLITUS [J].
ARCHER, AG ;
WATKINS, PJ ;
THOMAS, PK ;
SHARMA, AK ;
PAYAN, J .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1983, 46 (06) :491-499
[4]   SUBJECTIVE SLEEP DISTURBANCE IN CHRONIC BACK PAIN [J].
ATKINSON, JH ;
ANCOLIISRAEL, S ;
SLATER, MA ;
GARFIN, SR ;
GILLIN, JC .
CLINICAL JOURNAL OF PAIN, 1988, 4 (04) :225-232
[5]   Gabapentin for the symptomatic treatment of painful neuropathy in patients with diabetes mellitus - A randomized controlled trial [J].
Backonja, M ;
Beydoun, A ;
Edwards, KR ;
Schwartz, SL ;
Fonseca, V ;
Hes, M ;
LaMoreaux, L ;
Garofalo, E .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1998, 280 (21) :1831-1836
[6]   A PROSPECTIVE-STUDY OF PAINFUL SYMPTOMS, SMALL-FIBER FUNCTION AND PERIPHERAL VASCULAR-DISEASE IN CHRONIC PAINFUL DIABETIC NEUROPATHY [J].
BENBOW, SJ ;
CHAN, AW ;
BOWSHER, D ;
MACFARLANE, IA ;
WILLIAMS, G .
DIABETIC MEDICINE, 1994, 11 (01) :17-21
[7]  
BERRY D, 1990, STAT METHODOLOGY PHA, P403
[8]   Progress report on new antiepileptic drugs: a summary of the fourth Eilat conference (EILAT IV) [J].
Bialer, M ;
Johannessen, SI ;
Kupferberg, HJ ;
Levy, RH ;
Loiseau, P ;
Perucca, E .
EPILEPSY RESEARCH, 1999, 34 (01) :1-41
[9]   Antidepressants and anticonvulsants for diabetic neuropathy and postherpetic neuralgia: A quantitative systematic review [J].
Collins, SL ;
Moore, RA ;
McQuay, HJ ;
Wiffen, P .
JOURNAL OF PAIN AND SYMPTOM MANAGEMENT, 2000, 20 (06) :449-458
[10]  
Dooley DJ, 2000, J PHARMACOL EXP THER, V295, P1086