Status:
COMPLETED
Effect of Ketamine on Opioid-Induced Hyperalgesia
Lead Sponsor:
Massachusetts General Hospital
Conditions:
Pain
Chronic Pain
Eligibility:
All Genders
18-65 years
Phase:
NA
Brief Summary
The purpose of this study is to compare pain threshold, pain tolerance, and wind up, as measured by QST, before and after a single dose of ketamine infusion under two clinical conditions: chronic pain...
Detailed Description
We hypothesize that: 1. Chronic pain patients on chronic opioids would have a lower pain threshold and lower pain tolerance when compared to opioid naïve patients (patients with chronic pain with non...
Eligibility Criteria
Inclusion
- Inclusion Criteria for Group 1
- Subject will be between ages 18 to 65 years.
- Subject has a chronic pain condition for at least three months. This requirement is set in order to avoid the clinical uncertainty of an unstable pain condition and to minimize the study variation. Subjects should have a VAS pain score at 4 or above at the time of study.
- Subject is on a chronic opioid treatment regimen (e.g., morphine, fentanyl, oxycodone, methadone, hydromorphone, hydrocodone) for at least three months. There should have been no changes in the type and amount of opioid dose for at least one month. Only patients with a minimal daily dose of at least 60 mg morphine equianalgesic dose will be included.
- Inclusion Criteria for Group 2
- Subject who meets the criteria #1 \& #2 as listed for Group 1.
- Subject has not been on an opioid regimen for the last three or more months.
- Exclusion Criteria for all groups:
- Subject has an altered sensation at the skin site of QST (one of upper extremities).
- Subject has scar tissue or acute injury at the skin site of QST.
- Subject has neurological disease or a condition causing upper extremities or generalized polyneuropathy, such as diabetic neuropathy, alcoholic neuropathy, AIDS neuropathy, multiple sclerosis, amyotrophic lateral sclerosis, and post-stroke residual neurological deficits.
- Subject has a diagnosis of renal or liver failure.
- Subject has a diagnosis of unstable angina, congestive heart failure, cardiac arrythmias or myocardial infarction within 1 year.
- Subject is allergic to ketamine.
- Subject had recent therapy that may influence QST results, e.g., neuroablative procedure involving upper extremities within six-months or peripheral neurolytic block involving upper extremities within two-months.
- Subject has a confirmed diagnosis of and is under the care of a psychiatrist for major depression disorder, eating disorder; alcohol or drug dependence; or attention deficit hyperactivity disorder. Subject has any history of a confirmed diagnosis of bipolar disorder, schizophrenia, anxiety disorder or a psychotic disorder
- Subject is tested positive on drug urine screening test.
- Subject is pregnant or breast-feeding.
- \-
Exclusion
Key Trial Info
Start Date :
September 1 2008
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
April 1 2016
Estimated Enrollment :
79 Patients enrolled
Trial Details
Trial ID
NCT00833755
Start Date
September 1 2008
End Date
April 1 2016
Last Update
July 23 2020
Active Locations (1)
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1
Massachusetts General Hospital
Boston, Massachusetts, United States, 02114