NL-OMON55029已完成不适用
eurological and neuropsychological sequelae of Covid-19 infection - Nenesco
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 430
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18 至 99（—）
入选标准
- •In order to be eligible to participate in this study, a subject must meet all
- •of the following criteria:
- •- Objectified COVID-19 infection for which ICU or hospital admission was
- •necessary at one of the participating hospitals
- •- Age > 18 years
- •- Sufficient command of the Dutch language to follow test instructions and
- •understand questionnaires
- •- Informed consent.
- •Primary caregivers (if present):
- •- Primary caregiver (spouse or close family member who takes care of the
- •patient most) of a participant with COVID-19 infection as described above
- •- Age > 18 years
- •- Sufficient command of the Dutch language to understand questionnaires
- •- Informed consent.
- •Patients subgroup second/third wave :
- •- Objectified COVID-19 infection for which ICU or non-ICU hospital admission
- •was necessary at the MUMC+one of the participating hospitals
- •- Age > 18 years
- •- Sufficient command of the Dutch language to follow test instructions and
- •understand questionnaires
- •- Informed consent
- •- Treated with both dexamethasone and tocilizumab during ICU admission.
排除标准
- •A potential subject who meets any of the following criteria will be excluded
- •from participation in this study:
- •- objectified cognitive impairments before the hospital admission for the
- •COVID-19 infection
- •- an unexpected incident leading to severe neurological damage occurring after
- •hospital discharge (such as stroke or traumatic brain injury)
- •- contra-indications for MRI scanning (e.g. metal implants, cardiac pacemaker,
- •claustrophobia, pregnancy)
- •-- physical inability to independently travel to one of the participating
- •hospitals (e.g., bedridden patients).
- •Primary caregivers: no exclusion criteria.
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