跳至主要内容
临床试验/CTRI/2013/01/003298
CTRI/2013/01/003298进行中(未招募)未知

A Prospective, Longitudinal, Case Control, Observational Study of Cerebral Venous Sinus Thrombosis in Western Maharashtra, India. Risk Factors, Clinical Presentations and Complications. - CVST

Pfizer Limited0 个研究点目标入组 250 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
进行中(未招募)
入组人数
250

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

入选标准

  • •1.Males and females between 18 and 65 years of age.
  • •2.Cerebral venous thrombosis confirmed by cerebral angiography (with intra-arterial contrast injection) or magnetic resonance venography or computed tomographic venography.
  • •3.Patients or authorized representative must be able and willing to provide written informed consent.
  • •4.Patients who are willing to or likely to comply with all study requirements.
  • •Inclusion for Control Arm Subjects
  • •1.Age and gender matched healthy individuals from
  • •community or hospital patients with minor illnesses from general OPD without any neurological conditions or previous history of thrombosis or CVST who is willing to participate.
  • •2.Males and females between 18 and 65 years of age.
  • •3.Patients or authorized representative must be able and
  • •willing to provide written informed consent.
  • •4.Patients who are willing to or likely to comply with all study
  • •requirements.

排除标准

  • •1.Any known associated condition (such as cancer) with a poor short term (1 year) (terminal illness) prognosis independent of CVST.
  • •2.Recent ( < 2 weeks) major surgical procedure including head & brain surgery (does not include lumbar puncture) or severe cranial trauma.
  • •3.Patients who are unlikely to comply with protocol requirements (e.g., non-cooperative behavior, inability to attend the protocol visits).
  • •4.Patients who are currently participating or had participated in other interventional study for last 30 days prior to their enrollment.

研究者

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