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临床试验/RBR-2pcycpx
RBR-2pcycpx尚未招募未知

Sleep Promotion for patients undergoing Percutaneous Intervention for the treatment of Heart Disease: randomized clinical trial - PROSOCARD PROSOCARD - sleep promotion for patients undergoing percutaneous intervention to treat heart disease

niversidade de São Paulo0 个研究点开始时间: 2020年12月15日最近更新:
适应症

试验速览

阶段
未知
状态
尚未招募
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Intervention

入排标准

年龄范围
18Y 至 0(—)

入选标准

  • Age over 18 years, communication and comprehension skills preserved.

排除标准

  • Report of severe sleep disorder requiring daily treatment before hospitalization, such as sleep apnea, narcolepsy and chronic insomnia; presence of serious complication (aortic dissection, bleeding or stroke after the procedure) related to the treatment; presence of delirium as medical record evaluation; severe hearing and visual loss; history of neurological disease or diagnosed psychiatric disorders; admission to the Intensive Care Unit between 9:00 pm to 6:00 am after the percutaneous intervention procedure; treatment with mechanical ventilation; need for sedation during stay in the ICU, who are not fluent in the Portuguese language.

研究者

发起方
niversidade de São Paulo

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