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临床试验/NCT01795326
NCT01795326已完成不适用

Assessment of Physician Behavior Regarding Metabolic Monitoring of Patients Treated With SEROQUEL® (Quetiapine Fumarate) Tablets and SEROQUEL® (Quetiapine Fumarate) Extended Release Tablets in Selected Countries in the EU

AstraZeneca0 个研究点目标入组 800 人开始时间: 2013年6月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
AstraZeneca
入组人数
800
主要终点
Determination via survey whether physicians monitor weight at initiation of treatment with Seroquel or Seoquel XR and on a regular basis after initiating treatment.

研究概览

简要总结

A physician survey to document receipt of metabolic educational materials and assess behavior of physicians in following messages communicated through the educational materials

详细描述

Assessment of physician behavior regarding metabolic monitoring of patients treated with SEROQUEL® (quetiapine fumarate) Tablets and SEROQUEL® (quetiapine fumarate) Extended Release Tablets in selected countries in the EU

研究设计

研究类型
Observational
时间视角
Cross Sectional

入排标准

性别
All
接受健康志愿者

入选标准

  • Physicians targeted to receive the metabolic educational materials and either currently prescribe or have the potential to prescribe SEROQUEL® or SEROQUEL® XR.

排除标准

  • Physicians who have participated in a survey involving SEROQUEL® / SEROQUEL® XR in the past six months are not eligible to participate in this survey.

结局指标

主要结局

Determination via survey whether physicians monitor weight at initiation of treatment with Seroquel or Seoquel XR and on a regular basis after initiating treatment.

时间窗: Over 6- 8 weeks.

Determination via survey whether physicians or someone in their practice perform monitoring of patients treated with Seroquel or Seroquel XR for metabolic issues related to treatment; refer their patients to another physician for monitoring.

时间窗: Over 6- 8 weeks.

Determination via survey whether physicians monitor tests for hyperlipidemia in patients who are taking Seroquel or Seroquel XR.

时间窗: Over 6- 8 weeks.

Determination via survey whether physicians monitor for signs and symptoms of hyperglycemia in patients who are taking Seroquel or Seroquel XR.

时间窗: Over 6- 8 weeks.

Determination via survey whether physicians monitor blood glucose in patients with diabetes or monitor patients with risk factors for diabetes for worsening of glycemic control if they are taking Seroquel or Seroquel XR.

时间窗: Over 6- 8 weeks.

次要结局

  • Determination via survey whether physicians counsel patients taking with Seroquel or Seroquel XR on healthy eating, exercise, and healthy lifestyle improvements.(Over 6- 8 weeks.)
  • Determination via survey whether physicians received educational information relevant to the issues in the survey from AstraZeneca.(Over 6- 8 weeks.)
  • Determination via survey whether physicians read the educational information.(Over 6- 8 weeks.)

研究者

发起方
AstraZeneca
申办方类型
Industry
责任方
Sponsor

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