A randomized, crossover evaluation of methylphenidate in cancer patients receiving strong narcotics
β Scribed by Mary B. Wilwerding; Charles L. Loprinzi; James A. Mailliard; Judith R. O'Fallon; Angela W. Miser; Carol Haelst; Debra L. Barton; John F. Foley; Laurie M. Athmann
- Book ID
- 104742049
- Publisher
- Springer-Verlag
- Year
- 1995
- Tongue
- English
- Weight
- 357 KB
- Volume
- 3
- Category
- Article
- ISSN
- 0941-4355
No coin nor oath required. For personal study only.
β¦ Synopsis
Sedation may be a doselimiting side-effect of opioid therapy in some cancer patients. This study was designed to evaluate further the use of the psychostimulant, methylphenidate, an agent that has been reported to counteract opioid-induced sedation, in patients with cancer-related pain. Pa-tients receiving a stable dose of an opioid for cancer-related pain were recruited for this randomized, double-blind, crossover clinical trial. In addition to their regular dose of narcotics, they received 5 days of methylphenidate followed by 5 days of placebo, or vice versa. Our data did not definitively demonstrate any statistically significant benefit for methylphenidate, but did suggest that this drug could mildly decrease narcotic-induced drowsiness and could increase night-time sleep. These data, in conjunction with other published data, suggest that methylphenidate can counteract narcotic-induced daytime sedation to a limited degree.
π SIMILAR VOLUMES
In a randomized crossover study 57 cancer patients receiving chemotherapy with high emetic potential were treated with low-dose levonantradol or standard-dose metoclopramide and crossed over to the other antiemetic drug in the next identical chemotherapy cycle. In the 45 patients evaluable for treat