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临床试验/PER-068-10
PER-068-10已完成未知

International, Multicenter Study of a Twenty-eight Week, Open-label, Titrated Oral Lixivaptan Administration in Patients With Chronic Hyponatremia: Extension to Studies CK-LX3401, 3405, and 3430

Cardiokine Biopharma, LLC,0 个研究点目标入组 0 人开始时间: 2010年10月18日最近更新:

试验速览

阶段
未知
状态
已完成

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 100(—)
性别
All

入选标准

  • Age greater than or equal to 18 years
  • Ability to provide informed consent or assent.
  • Previous participation in a hyponatremia trial with lixivaptan with evidence of desire or need to continue therapy. Patients must have demonstrated acceptable compliance with the experimental medication (> 70% of the prescribed medication taken) and adherence to the study procedures in the original trial.

排除标准

  • A current medical condition for which long-term treatment with an aquatic agent may pose an undue risk to the patient.
  • Hyponatremia which is acute, reversible, artificial or caused by conditions not associated with excess vasopressin or that may respond to aquatic therapy.
  • Hyponatremia caused by a reversible medical therapy or condition
  • Conditions associated with an imminent independent risk of morbidity and mortality.

研究者

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