Postoperative cancer pain
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Cancer patient for surgery treatment 2) Pain controlled by oxycodone or fentanyl for over 1 month 3) Age over 20 yrs old 4) ASA Physical status 1 or 2 5) Not pregnant 6) Informed consent by his/her own will
Exclusion criteria
Exclusion criteria: 1) Opioid treatment for non-cancer pain 2) Hepatic failure (AST or ALT >300IU) 3) Renal failure (BUN>50 Cre>3.0) 4) Pregnant or breast feeding patient 5) Not applicable determined by the Dr responsible for the trial.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Effective pain control (Numerical Rating Scale at rest <5) with calculated opioid dose. | — |
Secondary
| Measure | Time frame |
|---|---|
| 1.Safety determined from the frequency of side-effects (respiratory depression, nausea, itching) in need of treatment. 2. Use of pain and respiratory threshold measurement in the calculation of opioid dosage. 3.Determination of Oxycodone po to iv ratio. | — |
Countries
Japan
Contacts
Chiba University Hospital Department of Anesthesiology and Palliative Medicine