NCT01867255已完成1 期
Pharmacokinetic Study Comparing Area Under the Curve for a Single Dose of Venlafaxine ER Pre- and Post-gastric Bypass
适应症
干预措施
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 发起方
- Mayo Clinic
- 入组人数
- 10
- 试验地点
- 1
- 主要终点
- Venlafaxine levels pre- and post-gastric bypass
研究概览
简要总结
The purpose of the study is to determine whether a significant and predictable change in bioavailability of extended-release venlafaxine occurs following Roux-en-Y gastric bypass.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Basic Science
- 盲法
- None
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
- 未提供
排除标准
- 未提供
研究组 & 干预措施
venlafaxine ER
Other
venlafaxine ER (extended-release) 75 mg once
干预措施: venlafaxine ER (extended-release) 75 mg (Drug)
结局指标
主要结局
Venlafaxine levels pre- and post-gastric bypass
时间窗: 3 to 4 months
This study will measure and compare venlafaxine and desvenlafaxine levels in participants before, and again 3 to 4 months after, gastric bypass surgery.
次要结局
未报告次要终点
研究者
研究点 (1)
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