A randomized, placebo-controlled trial of oxycodone and of gabapentin for acute pain in herpes zoster
Although acute pain in patients with herpes zoster can be severe and has a substantial impact on health-related quality of life, there have been no randomized clinical trials of oral medications specifically for its ongoing treatment. A randomized clinical trial was conducted in which 87 subjects ⩾5...
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Published in | Pain (Amsterdam) Vol. 142; no. 3; pp. 209 - 217 |
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Main Authors | , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Philadelphia, PA
Elsevier B.V
01.04.2009
Lippincott Williams & Wilkins, Inc Elsevier |
Subjects | |
Online Access | Get full text |
ISSN | 0304-3959 1872-6623 1872-6623 |
DOI | 10.1016/j.pain.2008.12.022 |
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Abstract | Although acute pain in patients with herpes zoster can be severe and has a substantial impact on health-related quality of life, there have been no randomized clinical trials of oral medications specifically for its ongoing treatment. A randomized clinical trial was conducted in which 87 subjects ⩾50 years of age with herpes zoster within 6 calendar days of rash onset and with worst pain in the past 24
h
⩾
3 on a 0–10 rating scale initiated 7 days of treatment with famciclovir in combination with 28 days of treatment with either controlled-release (CR) oxycodone, gabapentin, or placebo. Subjects were evaluated for adverse effects of treatment, acute pain, and health-related quality of life. The results showed that CR-oxycodone and gabapentin were generally safe and were associated with adverse events that reflect well-known effects of these medications. Discontinuing participation in the trial, primarily associated with constipation, occurred more frequently in subjects randomized to CR-oxycodone (27.6%) compared with placebo (6.9%). Treatment with CR-oxycodone reduced the mean worst pain over days 1–8 (
p
=
0.01) and days 1–14 (
p
=
0.02) relative to placebo but not throughout the entire 28-day treatment period as pain resolved in most subjects. Gabapentin did not provide significantly greater pain relief than placebo, although the data for the first week were consistent with a modest benefit. By demonstrating that CR-oxycodone is safe, generally adequately tolerated, and appears to have efficacy for relieving acute pain, the results of this clinical trial provide a foundation for evidence-based treatment for acute pain in herpes zoster. |
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AbstractList | Although acute pain in patients with herpes zoster can be severe and has a substantial impact on health-related quality of life, there have been no randomized clinical trials of oral medications specifically for its ongoing treatment. A randomized clinical trial was conducted in which 87 subjects ⩾50 years of age with herpes zoster within 6 calendar days of rash onset and with worst pain in the past 24
h
⩾
3 on a 0–10 rating scale initiated 7 days of treatment with famciclovir in combination with 28 days of treatment with either controlled-release (CR) oxycodone, gabapentin, or placebo. Subjects were evaluated for adverse effects of treatment, acute pain, and health-related quality of life. The results showed that CR-oxycodone and gabapentin were generally safe and were associated with adverse events that reflect well-known effects of these medications. Discontinuing participation in the trial, primarily associated with constipation, occurred more frequently in subjects randomized to CR-oxycodone (27.6%) compared with placebo (6.9%). Treatment with CR-oxycodone reduced the mean worst pain over days 1–8 (
p
=
0.01) and days 1–14 (
p
=
0.02) relative to placebo but not throughout the entire 28-day treatment period as pain resolved in most subjects. Gabapentin did not provide significantly greater pain relief than placebo, although the data for the first week were consistent with a modest benefit. By demonstrating that CR-oxycodone is safe, generally adequately tolerated, and appears to have efficacy for relieving acute pain, the results of this clinical trial provide a foundation for evidence-based treatment for acute pain in herpes zoster. Although acute pain in patients with herpes zoster can be severe and has a substantial impact on health-related quality of life, there have been no randomized clinical trials of oral medications specifically for its ongoing treatment. A randomized clinical trial was conducted in which 87 subjects >or=50 years of age with herpes zoster within 6 calendar days of rash onset and with worst pain in the past 24h >or=3 on a 0-10 rating scale initiated 7 days of treatment with famciclovir in combination with 28 days of treatment with either controlled-release (CR) oxycodone, gabapentin, or placebo. Subjects were evaluated for adverse effects of treatment, acute pain, and health-related quality of life. The results showed that CR-oxycodone and gabapentin were generally safe and were associated with adverse events that reflect well-known effects of these medications. Discontinuing participation in the trial, primarily associated with constipation, occurred more frequently in subjects randomized to CR-oxycodone (27.6%) compared with placebo (6.9%). Treatment with CR-oxycodone reduced the mean worst pain over days 1-8 (p=0.01) and days 1-14 (p=0.02) relative to placebo but not throughout the entire 28-day treatment period as pain resolved in most subjects. Gabapentin did not provide significantly greater pain relief than placebo, although the data for the first week were consistent with a modest benefit. By demonstrating that CR-oxycodone is safe, generally adequately tolerated, and appears to have efficacy for relieving acute pain, the results of this clinical trial provide a foundation for evidence-based treatment for acute pain in herpes zoster.Although acute pain in patients with herpes zoster can be severe and has a substantial impact on health-related quality of life, there have been no randomized clinical trials of oral medications specifically for its ongoing treatment. A randomized clinical trial was conducted in which 87 subjects >or=50 years of age with herpes zoster within 6 calendar days of rash onset and with worst pain in the past 24h >or=3 on a 0-10 rating scale initiated 7 days of treatment with famciclovir in combination with 28 days of treatment with either controlled-release (CR) oxycodone, gabapentin, or placebo. Subjects were evaluated for adverse effects of treatment, acute pain, and health-related quality of life. The results showed that CR-oxycodone and gabapentin were generally safe and were associated with adverse events that reflect well-known effects of these medications. Discontinuing participation in the trial, primarily associated with constipation, occurred more frequently in subjects randomized to CR-oxycodone (27.6%) compared with placebo (6.9%). Treatment with CR-oxycodone reduced the mean worst pain over days 1-8 (p=0.01) and days 1-14 (p=0.02) relative to placebo but not throughout the entire 28-day treatment period as pain resolved in most subjects. Gabapentin did not provide significantly greater pain relief than placebo, although the data for the first week were consistent with a modest benefit. By demonstrating that CR-oxycodone is safe, generally adequately tolerated, and appears to have efficacy for relieving acute pain, the results of this clinical trial provide a foundation for evidence-based treatment for acute pain in herpes zoster. Although acute pain in patients with herpes zoster can be severe and has a substantial impact on health-related quality of life, there have been no randomized clinical trials of oral medications specifically for its ongoing treatment. A randomized clinical trial was conducted in which 87 subjects >or=50 years of age with herpes zoster within 6 calendar days of rash onset and with worst pain in the past 24h >or=3 on a 0-10 rating scale initiated 7 days of treatment with famciclovir in combination with 28 days of treatment with either controlled-release (CR) oxycodone, gabapentin, or placebo. Subjects were evaluated for adverse effects of treatment, acute pain, and health-related quality of life. The results showed that CR-oxycodone and gabapentin were generally safe and were associated with adverse events that reflect well-known effects of these medications. Discontinuing participation in the trial, primarily associated with constipation, occurred more frequently in subjects randomized to CR-oxycodone (27.6%) compared with placebo (6.9%). Treatment with CR-oxycodone reduced the mean worst pain over days 1-8 (p=0.01) and days 1-14 (p=0.02) relative to placebo but not throughout the entire 28-day treatment period as pain resolved in most subjects. Gabapentin did not provide significantly greater pain relief than placebo, although the data for the first week were consistent with a modest benefit. By demonstrating that CR-oxycodone is safe, generally adequately tolerated, and appears to have efficacy for relieving acute pain, the results of this clinical trial provide a foundation for evidence-based treatment for acute pain in herpes zoster. |
Author | Gnann, John W. Kieburtz, Karl Dworkin, Robert H. Bennett, Gary J. Schmader, Kenneth E. Barbano, Richard L. Pennella-Vaughan, Janet Irvine, Carrie Berber, Erhan Kamp, Cornelia Max, Mitchell B. Betts, Robert F. McDermott, Michael P. Tyring, Stephen K. |
AuthorAffiliation | Departments of Anesthesiology and Neurology, University of Rochester School of Medicine and Dentistry, 601 Elmwood Avenue, Box 604, Rochester, NY 14642, USA Department of Neurology, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA Department of Dermatology, University of Texas Health Science Center and the Center for Clinical Studies, Houston, TX, USA Department of Medicine, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA Departments of Biostatistics and Computational Biology and Neurology, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA Department of Anesthesiology, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA Department of Anesthesiology, McGill University, Montreal, Canada Novartis Pharmaceuticals, East Hanover, NJ, USA Departments of Medicine, Pediatrics, and Microbiology, University of Alabama at Birmingham and Birmingham Veterans Administration Medicine Center, Bi |
AuthorAffiliation_xml | – name: Departments of Anesthesiology and Neurology, University of Rochester School of Medicine and Dentistry, 601 Elmwood Avenue, Box 604, Rochester, NY 14642, USA Department of Neurology, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA Department of Dermatology, University of Texas Health Science Center and the Center for Clinical Studies, Houston, TX, USA Department of Medicine, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA Departments of Biostatistics and Computational Biology and Neurology, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA Department of Anesthesiology, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA Department of Anesthesiology, McGill University, Montreal, Canada Novartis Pharmaceuticals, East Hanover, NJ, USA Departments of Medicine, Pediatrics, and Microbiology, University of Alabama at Birmingham and Birmingham Veterans Administration Medicine Center, Birmingham, AL, USA Department of Biostatistics and Computational Biology, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA Department of Anesthesiology, University of Pittsburgh, Pittsburgh, PA, USA Department of Medicine-Geriatrics, Duke University, and GRECC, Durham VA Medical Center, Durham, NC, USA |
Author_xml | – sequence: 1 givenname: Robert H. surname: Dworkin fullname: Dworkin, Robert H. email: robert_dworkin@urmc.rochester.edu organization: Departments of Anesthesiology and Neurology, University of Rochester School of Medicine and Dentistry, 601 Elmwood Avenue, Box 604, Rochester, NY 14642, USA – sequence: 2 givenname: Richard L. surname: Barbano fullname: Barbano, Richard L. organization: Department of Neurology, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA – sequence: 3 givenname: Stephen K. surname: Tyring fullname: Tyring, Stephen K. organization: Department of Dermatology, University of Texas Health Science Center and the Center for Clinical Studies, Houston, TX, USA – sequence: 4 givenname: Robert F. surname: Betts fullname: Betts, Robert F. organization: Department of Medicine, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA – sequence: 5 givenname: Michael P. surname: McDermott fullname: McDermott, Michael P. organization: Departments of Biostatistics and Computational Biology and Neurology, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA – sequence: 6 givenname: Janet surname: Pennella-Vaughan fullname: Pennella-Vaughan, Janet organization: Department of Anesthesiology, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA – sequence: 7 givenname: Gary J. surname: Bennett fullname: Bennett, Gary J. organization: Department of Anesthesiology, McGill University, Montreal, Canada – sequence: 8 givenname: Erhan surname: Berber fullname: Berber, Erhan organization: Novartis Pharmaceuticals, East Hanover, NJ, USA – sequence: 9 givenname: John W. surname: Gnann fullname: Gnann, John W. organization: Departments of Medicine, Pediatrics, and Microbiology, University of Alabama at Birmingham and Birmingham Veterans Administration Medicine Center, Birmingham, AL, USA – sequence: 10 givenname: Carrie surname: Irvine fullname: Irvine, Carrie organization: Department of Biostatistics and Computational Biology, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA – sequence: 11 givenname: Cornelia surname: Kamp fullname: Kamp, Cornelia organization: Department of Neurology, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA – sequence: 12 givenname: Karl surname: Kieburtz fullname: Kieburtz, Karl organization: Department of Neurology, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA – sequence: 13 givenname: Mitchell B. surname: Max fullname: Max, Mitchell B. organization: Department of Anesthesiology, University of Pittsburgh, Pittsburgh, PA, USA – sequence: 14 givenname: Kenneth E. surname: Schmader fullname: Schmader, Kenneth E. organization: Department of Medicine-Geriatrics, Duke University, and GRECC, Durham VA Medical Center, Durham, NC, USA |
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Keywords | Postherpetic neuralgia Herpes zoster Randomized clinical trial Acute pain Gabapentin Oxycodone Human Skin disease Nervous system diseases Evaluation scale Post-herpetic neuralgia Quality of life Infection Treatment Viral disease Placebo Clinical trial Release |
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SubjectTerms | Acute Disease Acute pain Aged Amines - therapeutic use Analgesics, Opioid - administration & dosage Biological and medical sciences Clinical Trials as Topic - trends Cyclohexanecarboxylic Acids - therapeutic use Delayed-Action Preparations - administration & dosage Evidence-Based Medicine - trends Female Fundamental and applied biological sciences. Psychology Gabapentin gamma-Aminobutyric Acid - therapeutic use Herpes zoster Herpes Zoster - drug therapy Herpes Zoster - epidemiology Humans Illness and personality Illness, stress and coping Male New York - epidemiology Oxycodone Oxycodone - administration & dosage Pain - drug therapy Pain - epidemiology Placebo Effect Postherpetic neuralgia Psychology and medicine Psychology. Psychoanalysis. Psychiatry Psychology. Psychophysiology Randomized clinical trial Somesthesis and somesthetic pathways (proprioception, exteroception, nociception); interoception; electrolocation. Sensory receptors Texas - epidemiology Treatment Outcome Vertebrates: nervous system and sense organs |
Title | A randomized, placebo-controlled trial of oxycodone and of gabapentin for acute pain in herpes zoster |
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