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Clinical Trial Summary

Cerebral vasospasm(CVS) after subarachnoid hemorrhage (SAH) results in a considerable amount of transient or even permanent neurological deficits and poor outcome of the patients. Transluminal Balloon angioplasty (TBA) or intraarterial application of vasodilators represents a rescue therapy for severe CVS. Indication, duration and efficacy of this treatment, however, is still under debate. Aim of the study is to investigate if such a rescue treatment can significantly reduce new delayed ischemic cerebral deficits after SAH. Hypothesis is that the occurance of delayed infarcts can be reduced by repetetive intraarterial therapy to more than 50 %.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01400360
Study type Interventional
Source Johann Wolfgang Goethe University Hospitals
Contact Hartmut Vatter, M. D.
Phone 069 / 6301
Email h.vatter@em.uni-frankfurt.de
Status Recruiting
Phase N/A
Start date August 2009

See also
  Status Clinical Trial Phase
Completed NCT00964548 - Safety Study of Dantrolene to Treat Cerebral Vasospasm After Subarachnoid Hemorrhage Phase 1/Phase 2