Opioid Dependence
Conditions
Keywords
opioid dependence, tolerant, dependent
Brief summary
This study seeks to determine the suitable doses of fentanyl with acceptable adverse effect and safety profile in opioid-dependent patients. The investigators anticipate that a well tolerated dose of fentanyl which produces demonstrable analgesia will be found and will be related to the patient's maintenance opioid dose.
Detailed description
Fentanyl is a synthetic opiate with a (clinical) potency of 50 to 100 times that of morphine. Because of its high lipid solubility, fentanyl has a rapid onset of action and a relatively short duration of action. Fentanyl is one of the most widely used agents in the synthetic opioids family. Being a pure agonist with no active metabolites, it is highly suitable for use in patients with opioid tolerance. It can be used outside of an intensive-care clinical environment. Evidence-based guidelines for clinicians on which agents to use, what doses should be considered and whether treatment doses are related to the dose and the pharmacological properties of the maintenance opioid are lacking, but needed. This study seeks to determine the suitable doses of fentanyl required in opioid-tolerant patients, which are able to overcome the tolerance and hyperalgesia while maintaining an acceptable therapeutic index. The importance of this study is that it has the potential to improve acute pain management in the opioid-tolerant population.
Interventions
DRUGFentanyl
Intravenous infusion using STANPUMP
Sponsors
University of Adelaide
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No
Inclusion criteria
1. Male or female, aged 18 to 65. 2. Maintained on any opioid with oral morphine equivalent daily dose (MEDD) of 60 mg and above. 3. Have adequate intravenous access for drug infusion. 4. Are currently abstaining from oral and intravenous recreational drug use.
Exclusion criteria
1. Known positive for Hepatitis B, Hepatitis C or HIV 2. Contraindication to cold pain testing e.g. cardiac or vascular disease especially Raynaud's phenomenon, blood pressure problems, diabetes, epilepsy and recent serious injury. 3. Using medication which affects pupil size e.g. glaucoma 4. Visual acuity poorer than 6 / 25 corrected (so that saccadic eye movements can be performed correctly. 5. Patients with respiratory insufficiency and poor respiratory drive. The criteria will be a spirometry reading of less than 70% the predicted value and/or having resting oxygen saturation levels of less than 95% on air. 6. Subject is pregnant and/or lactating. 7. Chronic use of benzodiazepines which cannot be withheld for 5 half-lives of the benzodiazepine the patient is on. 8. Known intolerance to fentanyl or other opioids 9. Patients taking tramadol. 10. Patients taking CYP3A4 inhibitors like amiodarone, azole antifungals, cimetidine, clarithromycin, cyclosporine, diltiazem, erythromycin, fluoroquinolones, grapefruit juice, HIV protease inhibitors, metronidazole, quinine, selective serotonin reuptake inhibitors (SSRIs) and tacrolimus. 11. A positive urine test for benzodiazepines on the day of screening or testing. 12. A positive breathalyzer test on the day of testing. 13. Creatinine clearance \< 30ml/min as estimated by Cockcroft-Gault formula. 14. Patients with bradyarrythmia.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Attainment of analgesia | Within 2 hours after starting the infusion | Attainment of analgesia as evidenced by having the cold pain tolerance test reading to twice the baseline value or reaching the absolute value of 2 minutes. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Pupillometry | Within 2 hours after infusion starts | The pupil diameter will be measured every 30 minutes during the infusion. |
| Saccadic eye movement | Within 2 hours after infusion starts | The average peak velocity of the saccadic eye movement will be measured every half an hour for 2 hours. |
| Morphine Benzedrine Group Scale | Within 2 hours after infusion starts | This paper test will take 3 minutes to complete and will measure the degree of euphoria. |
| Electroencephalography (EEG) | Within 2 hours after infusion starts | The delta, theta and alpha Fz-Cz and Pz-Oz activity will be measured every 30 minutes during the infusion. |
| Subjective Opioid Withdrawal Scale | Within 1 hour after infusion stops | This paper test will take 3 minutes to complete and will measure the degree of withdrawal. It will be done at 15, 30 and 60 minutes post infusion. |
Countries
Australia
Contacts
Primary ContactPaul E Rolan
Outcome results
None listed