跳至主要内容
临床试验/NCT01073579
NCT01073579已完成不适用

Sabril Patient Registry

Lundbeck LLC0 个研究点目标入组 9,423 人开始时间: 2009年8月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
Lundbeck LLC
入组人数
9,423
主要终点
Characterize the prevalence, incidence, time to onset, progression, and severity of vision loss during Sabril treatment.

研究概览

简要总结

The purpose of this study is to create a patient registry to collect and analyze information on subjects treated with Sabril and the prescribers of Sabril.

详细描述

This prospective registry is part of the overall Risk Evaluation and Mitigation Strategy (REMS) required for Sabril by the United States Food and Drug Administration (FDA). All physicians who prescribe Sabril and all patients who take Sabril will be enrolled in a H. Lundbeck A/S-sponsored program called "SHARE" (Support, Help and Resources for Epilepsy), and the data that are collected and entered into the SHARE database will form the basis of this patient registry.

Prior to any prescription being filled by one of the specialty pharmacies, the prescribing physician and the patient must be enrolled in SHARE. A call center (SHARE Call Center) will act as the hub for a network of select specialty pharmacies. Participation in both SHARE and the patient registry is mandatory.

Information regarding prescriber specialty and location, patient demographic and disease characteristics will be collected through SHARE and entered into the database. Patients will be assigned a unique patient identifier upon entry into the registry, and all data related to that patient will be associated with this identifier.

Early in therapy (within 2-4 weeks for Infantile Spasms patients and 3 months for adult refractory Complex Partial Seizures patients), a mandatory benefit/risk assessment will occur. If the benefit of Sabril therapy exceeds the risk of vision loss, the prescribing physician will complete and submit the appropriate SHARE form and the patient will continue into the maintenance therapy phase of treatment. The outcome of this benefit/risk assessment will be entered into the database.

Regular assessments of vision are required during Sabril therapy to contribute information related to the ongoing benefit/risk assessments. The required assessments will occur at baseline, every 3 months during therapy, and about 3-6 months after stopping Sabril. The visual assessment results will be recorded and submitted using the appropriate SHARE forms, and the data will be entered into the database. A copy of the visual field will be included.

研究设计

研究类型
Observational
时间视角
Prospective

入排标准

性别
All
接受健康志愿者

入选标准

  • All patients in the U.S. who are prescribed Sabril must participate in this patient registry in order to receive Sabril.

排除标准

  • 未提供

研究组 & 干预措施

Sabril®

All patients in the U.S. who are prescribed Sabril must participate in this patient registry in order to receive Sabril.

干预措施: Sabril® (Drug)

结局指标

主要结局

Characterize the prevalence, incidence, time to onset, progression, and severity of vision loss during Sabril treatment.

时间窗: A yearly report

次要结局

  • Characterize the physician specialties for prescribers of Sabril.(A yearly report)
  • Characterize the demographics, disease characteristics, dose and duration of therapy for patients who receive Sabril.(A yearly report)

研究者

发起方
Lundbeck LLC
申办方类型
Industry
责任方
Sponsor

相似试验