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临床试验/NCT03211091
NCT03211091Unknown不适用

Prove/Cerebrovascular Registry

Isfahan University of Medical Sciences0 个研究点目标入组 5,000 人开始时间: 2015年1月1日最近更新:
适应症

试验速览

阶段
不适用
入组人数
5,000
主要终点
disability

研究概览

简要总结

Patients with stroke were registered based on the WHO/ MONICA protocol and were followed-up for 28 days, starting in 2015 in PROVE Registry

详细描述

PROVE program started in 2015, the registration of stroke continued but followed the WHO Stepwise method instead of WHO/MONICA .Patients are followed up for two years. The corresponding questionnaire covered the patients' demographic data, medical history upon hospital admission, history of comorbidities, medications used prior to the treatment, history of drug abuse, heart and brain imaging, history of blood tests and blood diseases, hospital treatments received, hospitalization complications, medications prescribed at the time of discharge, discharge status and the definite diagnosis of type of stroke according to CT or MRI.

The patients were followed-up over the phone or in person from the 1st, 3rd and 12th months to two years. The patients' disabilities were measured using the Barthel Index and the Modified Rankin Scale (MRS). The reliability and validity of these two questionnaires have already been investigated in Persian. In addition, secondary prevention measures, rehabilitation status and the incidence of new cardiovascular events were also examined in the follow-up. The stroke registration personnel received an initial training of three two-hour sessions and monthly one-hour retraining sessions. They visited the archives of various hospitals on a daily basis and registered the data contained in the records

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
15 Years 至 90 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • * patients with acute Stroke (Hemorrhagic and Non Hemorrhagic)

排除标准

  • patients who do not agree to continue cooperation
  • patients with incomplete documents

结局指标

主要结局

disability

时间窗: 3 months

the Barthel Index

次要结局

  • rehabilitation(12 months)

研究者

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

Mohammad Saadatnia

Professor Mohammad Saadatnia

Isfahan University of Medical Sciences

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