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临床试验/NCT00889135
NCT00889135Approved For Marketing不适用

Long Term Treatment With L-DOPS

Vanderbilt University1 个研究点 分布在 1 个国家开始时间: 2004年9月最近更新:
适应症

试验速览

阶段
不适用
状态
Approved For Marketing
试验地点
1

研究概览

简要总结

This study is designed to supply L-DOPS (droxidopa) on a long term basis to patients with a genetic form of profound orthostatic hypotension, most commonly DBH deficiency. It also allows us to collect medical history information on this small population of patients that would allow us to determine if there are any complications from this type of treatment.

研究设计

研究类型
Expanded Access

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

  • 18 years old or older with orthostatic hypotension
  • established diagnosis of DBH deficiency and fractionated plasma catecholamine levels that show high dopamine levels and very low norepinephrine and epinephrine levels. Blood pressure increase in response to oral treatment with L-DOPS during previous studies.

排除标准

  • subjects with orthostatic hypotension that do not have a genetic form of the disorder and catecholamine pattern is not consistent with that above.

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

David Robertson

Professor of Medicine and Pharmacology

Vanderbilt University

研究点 (1)

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