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No enough recruitments, very slow enrollment over the years
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The purpose of this research is to determine the pain-reducing effects of ketamine (Ketalar, an FDA-approved drug for anesthesia) and methadone (Dolophine, a long-acting narcotic) after lumbar laminectomy. The investigators would like to evaluate whether intraoperative use of both drugs may be able to provide better control of pain after lumbar surgery.
During and after the surgery, patients undergoing surgery most likely need narcotics (opioids) that can cause side effects such as drowsiness and constipation. This can delay your recovery. The investigator would like to determine if the intraoperative use of ketamine and methadone will provide better pain control and reduce the use of narcotic painkiller medications (analgesics) after lumbar surgery as compared to either drug (ketamine or methadone) alone.
Ketamine is used to help to reduce the amount of the commonly used intravenous anesthetic drugs, minimize heart rate and blood pressure instability during surgery, and to improve outcomes after surgery (e.g. less pain, less constipation, less nausea and vomiting after surgery, faster return of bowel function and shortened length of hospital stay).
Ketamine is approved by the U.S. Food and Drug Administration (FDA) to be used: as an anesthetic and analgesic (painkiller). Ketamine is an "adjuvant," which is a drug that may increase the effectiveness or strength of other drugs when given at the same time. Ketamine is administered as an adjuvant during anesthesia to produce anesthetic and analgesic-sparing effects (reduce the amount of anesthetics and narcotics-painkiller drugs), hemodynamic stability (to maintain the blood pressure and heart rate within normal rank) and side effect reduction (e.g., constipation, nausea and vomiting, itching, and urinary retention). Ketamine will be used as approved in this study. Ketamine is frequently used intraoperatively for pain control in patients undergoing spine surgery at our institution and is within the standard of care. The standard of care indicates that this is one possible method which has been demonstrated to be safe and effective for patient care. This may vary at different institutions.
Methadone is approved by the U.S. Food and Drug Administration (FDA) to be used: as an opioid pain reliever, similar to morphine, and for narcotic detoxification to reduce withdrawal symptoms. The dose of methadone that will be used in this study may be slightly higher than the approved dose depending on the subject's weight. However, this dose of methadone is frequently used intraoperatively for pain control in patients undergoing spine surgery at our institution and is within the standard of care. This may vary at different institutions.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Ketamine | Active Comparator | A bolus of intravenous (IV) ketamine during induction (0.5mg/kg), and an IV infusion of ketamine intraoperatively (5 mcg/kg/min)) |
|
| Methadone | Active Comparator | Will receive a single dose of IV methadone (0.2 mg/kg) preinduction |
|
| Ketamine + methadone | Experimental | Methadone (0.2 mg/kg) preinduction, a bolus of IV ketamine (0.5 mg/kg) during induction and IV ketamine infusion intraoperatively (5 mcg/kg/min) |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Ketamine | Drug | A bolus of intravenous (IV) ketamine during induction (0.5mg/kg), and an IV infusion of ketamine intraoperatively (5 mcg/kg/min) |
|
| Measure | Description | Time Frame |
|---|---|---|
| Opioid Consumption Obtained From the Recorded Data | Perioperative use of opioid consumption inside the hospital (recorded by study staff and data obtained from patient charts) | 1 day |
| Postoperative Pain | Postoperative pain was measured at PACU using a Verbal Rating Scale from 0 to 10. Where 0= no pain and 10= maximum pain experienced | 1 day |
| Measure | Description | Time Frame |
|---|---|---|
| Nausea and Vomiting | The number of participants who experienced nausea and vomiting | 1 day |
| Number of Participants With Constipation at Follow up | Day one, day three after surgery |
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Inclusion Criteria:
• 18 - 80 years old of either gender, scheduled for elective lumbar laminectomy
Exclusion Criteria:
American Society of Anesthesiologists (ASA) IV and above
Intolerance, allergy, or contraindication to use of any medications used in this study
Significant coronary artery disease (abnormal stress test, myocardial infarction
Increased intraocular pressure (e.g., untreated glaucoma)
Uncontrolled hypertension (BP > 140/90)
Sleep apnea and currently on continuous positive airway pressure (CPAP)
Increased intracranial pressure or clinical signs thereof
History of intracranial surgery, stroke, or brain aneurysm
Cardiac arrhythmias particularly prolonged QT syndrome
Drugs known to cause prolonged qT: class (IA) antiarrhythmics (quinidine, procainamide, disopyramide), class III antiarrhythmics (sotalol, dofetilide, ibutilide, amiodarone), haloperidol, thioridazine, arsenic trioxide, HIV protease inhibitors, tricyclic antidepressants
Individuals with significant psychological disorders including: schizophrenia, mania, bipolar disorder or psychosis
Pregnant or lactating women
Emergent laminectomy
Those already receiving ketamine or methadone prior to surgery
Morbid obesity (BMI > 40 kg/m2) AND/OR weight > 150 kg
Chronic renal failure ( creatinine > 2.0 mg/dL)
Liver failure e.g., active cirrhosis
Alcohol or substance abuse within in the past 3 months
Uncorrected hypokalemia, hypomagnesemia, hypocalcemia (can be due to diuretics, mineralocorticoid use, laxatives)
Chronic obstructive pulmonary disease (COPD)/Hypercarbia
Restrictive lung disease (pulmonary fibrosis, myasthenia gravis)
Congestive heart failure
Thyroid disease
Organ transplant patients
Drugs/substances known to inhibit methadone metabolism: macrolide antibiotics e.g., erythromycin, cimetidine, astemizole, voriconazole, grapefruit juice
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| Name | Affiliation | Role |
|---|---|---|
| Roya Yumul, M.D., PhD. | Cedars-Sinai Medical Center | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Cedars Sinai Medical Center | Los Angeles | California | 90048 | United States |
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| ID | Title | Description |
|---|---|---|
| FG000 | Ketamine | A bolus of intravenous (IV) ketamine during induction (0.5mg/kg), and an IV infusion of ketamine intraoperatively (5 mcg/kg/min)) Methadone: A single dose of IV methadone (0.2 mg/kg) preinduction. Ketamine + methadone: Methadone (0.2 mg/kg) preinduction, a bolus of IV ketamine (0.5 mg/kg) during induction and IV ketamine infusion intraoperatively (5 mcg/kg/min) |
| FG001 | Methadone | Will receive a single dose of IV methadone (0.2 mg/kg) preinduction Ketamine: A bolus of intravenous (IV) ketamine during induction (0.5mg/kg), and an IV infusion of ketamine intraoperatively (5 mcg/kg/min) Ketamine + methadone: Methadone (0.2 mg/kg) preinduction, a bolus of IV ketamine (0.5 mg/kg) during induction and IV ketamine infusion intraoperatively (5 mcg/kg/min) |
| FG002 | Ketamine + Methadone | Methadone (0.2 mg/kg) preinduction, a bolus of IV ketamine (0.5 mg/kg) during induction and IV ketamine infusion intraoperatively (5 mcg/kg/min) Ketamine: A bolus of intravenous (IV) ketamine during induction (0.5mg/kg), and an IV infusion of ketamine intraoperatively (5 mcg/kg/min) Methadone: A single dose of IV methadone (0.2 mg/kg) preinduction. |
| Title | Milestones | Reasons Not Completed | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
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| ID | Title | Description |
|---|---|---|
| BG000 | Ketamine | A bolus of intravenous (IV) ketamine during induction (0.5mg/kg), and an IV infusion of ketamine intraoperatively (5 mcg/kg/min)) Methadone: A single dose of IV methadone (0.2 mg/kg) preinduction. Ketamine + methadone: Methadone (0.2 mg/kg) preinduction, a bolus of IV ketamine (0.5 mg/kg) during induction and IV ketamine infusion intraoperatively (5 mcg/kg/min) |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Categorical | Count of Participants |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Opioid Consumption Obtained From the Recorded Data | Perioperative use of opioid consumption inside the hospital (recorded by study staff and data obtained from patient charts) | Posted | Mean | Standard Deviation | milligram morphine equivalents | 1 day |
|
six weeks
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Ketamine | A bolus of intravenous (IV) ketamine during induction (0.5mg/kg), and an IV infusion of ketamine intraoperatively (5 mcg/kg/min)) Methadone: A single dose of IV methadone (0.2 mg/kg) preinduction. Ketamine + methadone: Methadone (0.2 mg/kg) preinduction, a bolus of IV ketamine (0.5 mg/kg) during induction and IV ketamine infusion intraoperatively (5 mcg/kg/min) |
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| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Ofelia Loani Elvir Lazo, MD | Cedars Sinai Medical Center | 310-423-1682 | Loani.Elvir-Lazo@cshs.org |
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot_SAP | Yes | Yes | No | Study Protocol and Statistical Analysis Plan | Feb 15, 2020 | Jan 16, 2024 | Prot_SAP_000.pdf |
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| ID | Term |
|---|---|
| D010149 | Pain, Postoperative |
| ID | Term |
|---|---|
| D011183 | Postoperative Complications |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D010146 | Pain |
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| ID | Term |
|---|---|
| D007649 | Ketamine |
| D008691 | Methadone |
| ID | Term |
|---|---|
| D003510 | Cyclohexanes |
| D003516 | Cycloparaffins |
| D006840 | Hydrocarbons, Alicyclic |
| D006844 | Hydrocarbons, Cyclic |
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| Methadone | Drug | A single dose of IV methadone (0.2 mg/kg) preinduction. |
|
| Ketamine + methadone | Drug | Methadone (0.2 mg/kg) preinduction, a bolus of IV ketamine (0.5 mg/kg) during induction and IV ketamine infusion intraoperatively (5 mcg/kg/min) |
|
| 3 days |
| BG001 | Methadone | Will receive a single dose of IV methadone (0.2 mg/kg) preinduction Ketamine: A bolus of intravenous (IV) ketamine during induction (0.5mg/kg), and an IV infusion of ketamine intraoperatively (5 mcg/kg/min) Ketamine + methadone: Methadone (0.2 mg/kg) preinduction, a bolus of IV ketamine (0.5 mg/kg) during induction and IV ketamine infusion intraoperatively (5 mcg/kg/min) |
| BG002 | Ketamine + Methadone | Methadone (0.2 mg/kg) preinduction, a bolus of IV ketamine (0.5 mg/kg) during induction and IV ketamine infusion intraoperatively (5 mcg/kg/min) Ketamine: A bolus of intravenous (IV) ketamine during induction (0.5mg/kg), and an IV infusion of ketamine intraoperatively (5 mcg/kg/min) Methadone: A single dose of IV methadone (0.2 mg/kg) preinduction. |
| BG003 | Total | Total of all reporting groups |
| Participants |
|
| Sex: Female, Male | Count of Participants | Participants |
|
| Race (NIH/OMB) | Count of Participants | Participants |
|
| Region of Enrollment | Count of Participants | Participants |
|
| OG002 | Ketamine + Methadone | Methadone (0.2 mg/kg) preinduction, a bolus of IV ketamine (0.5 mg/kg) during induction and IV ketamine infusion intraoperatively (5 mcg/kg/min) Ketamine: A bolus of intravenous (IV) ketamine during induction (0.5mg/kg), and an IV infusion of ketamine intraoperatively (5 mcg/kg/min) Methadone: A single dose of IV methadone (0.2 mg/kg) preinduction. |
|
|
| Primary | Postoperative Pain | Postoperative pain was measured at PACU using a Verbal Rating Scale from 0 to 10. Where 0= no pain and 10= maximum pain experienced | Posted | Mean | Standard Deviation | score on a scale | 1 day |
|
|
|
| Secondary | Nausea and Vomiting | The number of participants who experienced nausea and vomiting | Posted | Count of Participants | Participants | 1 day |
|
|
|
| Secondary | Number of Participants With Constipation at Follow up | Day one, day three after surgery | Posted | Count of Participants | Participants | 3 days |
|
|
|
| 0 |
| 5 |
| 0 |
| 5 |
| 0 |
| 5 |
| EG001 | Methadone | Will receive a single dose of IV methadone (0.2 mg/kg) preinduction Ketamine: A bolus of intravenous (IV) ketamine during induction (0.5mg/kg), and an IV infusion of ketamine intraoperatively (5 mcg/kg/min) Ketamine + methadone: Methadone (0.2 mg/kg) preinduction, a bolus of IV ketamine (0.5 mg/kg) during induction and IV ketamine infusion intraoperatively (5 mcg/kg/min) | 0 | 6 | 0 | 6 | 0 | 6 |
| EG002 | Ketamine + Methadone | Methadone (0.2 mg/kg) preinduction, a bolus of IV ketamine (0.5 mg/kg) during induction and IV ketamine infusion intraoperatively (5 mcg/kg/min) Ketamine: A bolus of intravenous (IV) ketamine during induction (0.5mg/kg), and an IV infusion of ketamine intraoperatively (5 mcg/kg/min) Methadone: A single dose of IV methadone (0.2 mg/kg) preinduction. | 0 | 2 | 0 | 2 | 0 | 2 |
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| D009461 | Neurologic Manifestations |
| D012816 | Signs and Symptoms |
| D006838 |
| Hydrocarbons |
| D009930 | Organic Chemicals |
| D007659 | Ketones |