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Clinical Trials List

Protocol NumberA0081063
Completed

2006-06-01 - 2008-06-30

Phase I

Terminated3

ICD-10I69.092

Facial weakness following nontraumatic subarachnoid hemorrhage

ICD-10I69.093

Ataxia following nontraumatic subarachnoid hemorrhage

ICD-10I69.098

Other sequelae following nontraumatic subarachnoid hemorrhage

ICD-10I69.192

Facial weakness following nontraumatic intracerebral hemorrhage

ICD-10I69.193

Ataxia following nontraumatic intracerebral hemorrhage

ICD-10I69.198

Other sequelae of nontraumatic intracerebral hemorrhage

ICD-10I69.292

Facial weakness following other nontraumatic intracranial hemorrhage

ICD-10I69.293

Ataxia following other nontraumatic intracranial hemorrhage

ICD-10I69.298

Other sequelae of other nontraumatic intracranial hemorrhage

ICD-10I69.392

Facial weakness following cerebral infarction

ICD-10I69.393

Ataxia following cerebral infarction

ICD-10I69.398

Other sequelae of cerebral infarction

ICD-10I69.892

Facial weakness following other cerebrovascular disease

ICD-10I69.893

Ataxia following other cerebrovascular disease

ICD-10I69.898

Other sequelae of other cerebrovascular disease

ICD-10I69.992

Facial weakness following unspecified cerebrovascular disease

ICD-10I69.993

Ataxia following unspecified cerebrovascular disease

ICD-10I69.998

Other sequelae following unspecified cerebrovascular disease

ICD-9438.89

Other late effects of cerebrovascular disease

  • Sponsor

  • Trial scale

    Multi-Regional Multi-Center

  • Update

    2026/02/01

Investigators and Locations

Principal Investigator 劉祥仁 Division of Neurology

Co-Principal Investigator

The Actual Total Number of Participants Enrolled

0 Terminated

Principal Investigator 胡漢華 Division of Neurology

Co-Principal Investigator

The Actual Total Number of Participants Enrolled

0 Terminated

Principal Investigator 張鳴宏 Division of Neurology

Co-Principal Investigator

The Actual Total Number of Participants Enrolled

0 Terminated

Condition/Disease

Objectives

Test Drug

Active Ingredient

Dosage Form

Dosage

Endpoints

Inclution Criteria

The Estimated Number of Participants

  • Taiwan

    30 participants

  • Global

    226 participants