Awardee OrganizationUNIVERSITY OF CALIFORNIA, SAN FRANCISCO
Description
Abstract Text
DESCRIPTION (Applicant?s abstract): 1. We will test the hypothesis that
underlying pain mechanism is a determinant of opioid sensitivity by
simultaneously measuring in both neuropathic and non-neuropathic chronic pain
patients the response of experimentally induced pain and ongoing clinical pain
to I.V. remifentanyl infusion. For experimental pain, we will use a model which
combine non-injurious heating and topical capsaicin to produce stable areas of
cutaneous secondary hyperalgesia. In health volunteers, this model is opioid
responsive. Study 1 is a two session, placebo-controlled study of the effect on
experimental and clinical pain of brief infusions of the high efficacy,
ultra-short acting opioid remifentanyl in 60 non-opioid using chronic pain
patients.
2. In study 2 we will determine whether a prolonged I.V. remifentanyl infusion
in opioid-naïve volunteers will produce acute analgesic tolerance to both
noxious thermal stimulation and experimentally induced cutaneous secondary
hyperalgesia. We will then test patients with ongoing chronic pain.
Demonstrating the simultaneous development of acute analgesic tolerance to
experimental pain and chronic pain would indicate that analgesic tolerance is
possible during long term opioid therapy. If acute tolerance develops, physical
dependence in the form of withdrawal symptoms, hyperalgesia to noxious stimuli,
and a rebound increase in pain over pretreatment levels may follow the
remifentanyl infusion.
3. Analgesic tolerance has been shown to develop during long term opioid
therapy of chronic non-malignant pain. In Study 3, non-opioid using chronic
pain patients will undergo a placebo-controlled study of the analgesic effect
of I.V. remifentanyl on acute experimental and chronic pain before and
following a 9 week, randomized parallel design, double-blind trial. Forty
subjects will receive the opioid hydromorphone and a control group of 20 will
receive the tricyclic antidepressant amitriptyline. At the end of the initial 3
week titration period and again after 6 weeks of fixed dosing, the I.V.
remifentanyl infusion will be repeated to reconstruct the dose-response curve
for experimental and chronic pain.
National Institute of Neurological Disorders and Stroke
CFDA Code
DUNS Number
094878337
UEI
KMH5K9V7S518
Project Start Date
01-January-2002
Project End Date
31-December-2002
Budget Start Date
Budget End Date
Project Funding Information for 2002
Total Funding
$188,502
Direct Costs
$188,502
Indirect Costs
Year
Funding IC
FY Total Cost by IC
2002
National Institute of Neurological Disorders and Stroke
$188,502
Year
Funding IC
FY Total Cost by IC
Sub Projects
No Sub Projects information available for 5P50NS021445-18 0006
Publications
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Clinical Studies
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