跳至主要内容
临床试验/NCT04173858
NCT04173858已完成不适用

Evaluation of the Quality of Life of Patients With Opioid-induced Constipation Under Treatment With Naloxegol. A One-year Follow-up Study

Kyowa Kirin Farmacéutica S.L.U.1 个研究点 分布在 1 个国家目标入组 126 人开始时间: 2017年9月21日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
126
试验地点
1
主要终点
Assessment of Quality of Life

研究概览

简要总结

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.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Diagnosis of Cancer
  • Treatment with opioids
  • OIC symptoms
  • Inadequate response to laxatives
  • Karnofsky equal or above 50
  • Ambulatory
  • Must be able to complete questionnaire forms

排除标准

  • at the start of the study:
  • Hypersensitivity to Naloxegol or vehicle
  • Suspicion or high risk of gastrointestinal block
  • High risk of GI perforation
  • Severe liver failure
  • Pregnancy or breastfeeding
  • Use of potent CYP3A4 inhibitors
  • Cognitive impairment

研究组 & 干预措施

Experimental

Patients with confirmed opioid-induced constipation diagnosis and inadequate response to laxatives.

干预措施: Naloxegol (Drug)

结局指标

主要结局

Assessment of Quality of Life

时间窗: 12 months

Patient Assessment of Constipation Quality of Life (PAC-QoL) Questionnaire

次要结局

  • Assessment of Constipation Symptoms(6 months)

研究者

发起方
Kyowa Kirin Farmacéutica S.L.U.
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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