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This project is a pilot study to evaluate the analgesic and opioid-sparing effects of ketamine in an ultra-low dose oral formulation as a novel intervention for treatment of chronic non-cancer pain in opioid-tolerant patients in the primary care outpatient setting.
Chronic pain is a major national public health issue, affecting about 100 million adults in the United States. Opioid pain medications are commonly used for treatment of chronic pain, but their use is fraught with consequences including an increasing prevalence of misuse, abuse, and overdose death, and side effects which lead to a reduced quality of life. An effective and safe medication that would improve control of chronic pain while reducing reliance on opioid medications would be valuable for patients, medical providers and society at large.
Ketamine, commonly used as an intravenous anesthetic agent, has been shown to have analgesic and opioid-sparing effects in the peri-operative period and in the palliative care setting. Based on promising preliminary data from an open-label treatment trial, this project is a pilot study to evaluate the analgesic and opioid-sparing effects of ketamine in an ultra-low dose oral formulation as a novel intervention for treatment of chronic non-cancer pain in the primary care outpatient setting.
The design of the proposed study is a randomized controlled two week parallel-group trial, with 32 patients receiving either the active treatment or placebo twice daily.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Active Drug | Active Comparator | ketamine 16 mg in flavored syrup by mouth twice daily for 1 week, then ketaming 32 mg in flavored syrup by mouth twice daily for 1 week |
|
| Placebo | Placebo Comparator | Flavored syrup (without ketamine) by mouth twice daily for 2 weeks |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Ketamine | Drug | ultra-low dose oral ketamine twice daily in two different doses over a 2 week period. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Pain improvement (Brief Pain Inventory (BPI) Mean Pain Severity Scale) | Improvement after 2 weeks in pain as measured by the Brief Pain Inventory (BPI) Mean Pain Severity Scale | 2 weeks |
| Function improvement (BPI Mean Interference Scale) | Improvement after 2 weeks in functional status as measured by the BPI Mean Interference Scale | 2 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Reduction in opioid use (self-reported average opioid dose) | Reduction after two weeks in self-reported average opioid dose, converted to morphine equivalents. | 2 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Reduction in depression (PHQ-9 depression score) | Reduction in depression, using the PHQ-9 depression score | 2 weeks |
Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Lucinda Grande, MD | University of Washington Department of Family Medicine | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Pioneer Family Practice | Lacey | Washington | 98503 | United States |
| Type | Date | Date Unknown |
|---|---|---|
| Release | Jul 8, 2018 | |
| Reset | Jul 31, 2018 | |
| Release | Jan 16, 2019 | |
| Reset | Feb 6, 2019 |
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| Release Date | Unrelease Date | Unrelease Date Unknown | Reset Date | MCP Release Number |
|---|---|---|---|---|
| Jul 8, 2018 | Jul 31, 2018 | |||
| Jan 16, 2019 |
| ID | Term |
|---|---|
| D059350 | Chronic Pain |
| ID | Term |
|---|---|
| D010146 | Pain |
| D009461 | Neurologic Manifestations |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |
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| ID | Term |
|---|---|
| D007649 | Ketamine |
| ID | Term |
|---|---|
| D003510 | Cyclohexanes |
| D003516 | Cycloparaffins |
| D006840 | Hydrocarbons, Alicyclic |
| D006844 | Hydrocarbons, Cyclic |
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| Feb 6, 2019 |
| D006838 |
| Hydrocarbons |
| D009930 | Organic Chemicals |