Opioid-induced constipation (OIC) is a common feature in patients treated with strong opioids. Such medication is often prescribed together with a laxative (osmotic, emollient), with effectiveness depending on the individual patient. Peripherally-acting, mu-opioid receptor antagonists (PAMORAs), such as Naloxegol, have proven to be effective against OIC in patients with inadequate response to laxatives without reducing opioid analgesic effect. However, evidence regarding efficacy and safety on patients with cancer is still scarce. The objective of this study was to analyze the efficacy of naloxegol in a real-world setting by assessing Quality of Life outcomes, and to obtain data on its safety in the long term in patients with cancer.
Study Type
OBSERVATIONAL
Enrollment
126
25 mg oral naloxegol once daily.
Hospital Universitario de Torrejon
Torrejón de Ardoz, Madrid, Spain
Assessment of Quality of Life
Patient Assessment of Constipation Quality of Life (PAC-QoL) Questionnaire
Time frame: 12 months
Assessment of Constipation Symptoms
Patient Assessment of Constipation Symptoms (PAC-SYM) Questionnaire
Time frame: 15 days
Assessment of Constipation Symptoms
Patient Assessment of Constipation Symptoms (PAC-SYM) Questionnaire
Time frame: 1 month
Assessment of Constipation Symptoms
Patient Assessment of Constipation Symptoms (PAC-SYM) Questionnaire
Time frame: 3 months
Assessment of Constipation Symptoms
Patient Assessment of Constipation Symptoms (PAC-SYM) Questionnaire
Time frame: 6 months
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