Evaluation of Function And Satisfaction of UbrogepanT-treated Migraine Patients in Canada (FAST): Prospective, Observational, Real-world Study
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 178
- 试验地点
- 19
- 主要终点
- Percentage of Participants Achieving Functional Disability Scale (FDS) Score of =0, no disability, able to function normally 4 hours post-dose
研究概览
简要总结
Migraine is a neurological disease characterized by moderate or severe headache, associated with nausea, vomiting, and/or sensitivity to light and sound. This study will evaluate function and satisfaction with oral ubrogepant in treating adult participants after multiple migraine attacks.
Ubrogepant is a drug approved for the acute treatment of migraine in adults. Approximately 167 participants will be enrolled in approximately 10-15 sites across Canada.
Participants will receive ubrogepant as prescribed by their physician according to their routine clinical practice and local label. Participants will be followed for up to 12 weeks.
There is expected to be no additional burden for participants in this trial. Participants will attend regular visits during the study at a hospital or clinic according to their routine clinical practice.
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
- 否
入选标准
- •Participants able to give voluntary informed consent before starting any study-related assessments or procedures (to be obtained/documented as per local regulations).
- •Adults (≥18 years of age) at time of informed consent.
- •Participants with at least 1-year history of migraine with or without aura consistent with a diagnosis according to the ICHD-3 (2018).
- •Participants with history of experiencing at least 3 migraine attacks per month with moderate to severe symptoms
- •Participants prescribed ubrogepant by investigator for the acute treatment of migraine according to local product label, independent of and prior to study participation
- •Participants willing and able to comply with the requirements of the study.
- •Participants with access to an electronic device (mobile phone, tablet, laptop, etc.) with internet access.
排除标准
- •Participants previously exposed to a ubrogepant or rimegepant as routine therapy or through a clinical trial.
- •Participants with history of known contraindications to ubrogepant as per local labeling.
- •Participants Pregnant or planning to be pregnant or of childbearing potential not using contraception
- •Participants enrolled in any interventional studies that may include investigational compounds for migraine or non-AbbVie observational studies.
- •History or current evidence of any condition that might interfere with their ability to comply with the study requirements, in the opinion of the investigator.
研究组 & 干预措施
Ubrogepant
Participants will receive Ubrogepant as prescribed by their physician in routine clinical practice.
结局指标
主要结局
Percentage of Participants Achieving Functional Disability Scale (FDS) Score of =0, no disability, able to function normally 4 hours post-dose
时间窗: Up to approximately 12 weeks
Functional Disability Scale (FDS) is a Patient-Reported Outcome (PRO) assessing the ability of a participant to perform daily activities, rated on a 4-point scale (0=no disability, able to function normally; to 3=severely impaired, cannot do all or most things, bed rest may be necessary)
次要结局
未报告次要终点