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Clinical Trial Summary

Although generalized convulsive status epilepticus (GCSE) is a life-threatening emergency, evidence-based data to guide initial drug treatment choices are lacking in the Chinese population. The investigators conduct this prospective randomized controlled trial to evaluate the relative efficacy and safety of intravenous (IV) phenobarbital (PB) and valproate (VPA) in patients with GCSE.


Clinical Trial Description

After the failure of first-line diazepam treatment, patients with GCSE are randomized to receive either IV PB (standard doses, low rate) or VPA (standard). Successful treatment is considered when clinical and electroencephalographic seizure activity ceases. Adverse events following treatment and the neurological outcomes at discharge and 3 months later are also evaluated. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03025906
Study type Interventional
Source Xuanwu Hospital, Beijing
Contact Su Yingying
Phone 15901361953
Email tangsuyingying@sina.com
Status Recruiting
Phase Phase 2
Start date February 16, 2017
Completion date December 2019

See also
  Status Clinical Trial Phase
Recruiting NCT05779657 - Combined Ketamine and Midazolam for Generalized Convulsive Status Epilepticus Phase 2/Phase 3
Completed NCT04926844 - Effectiveness of Combined Levetiracetam and Midazolam in Generalized Convulsive Status Epilepticus in Children Phase 2
Completed NCT01791868 - Efficacy Study of Intravenous Sodium Valproate in Addition to First Line Anti Epileptic Treatment of Generalized Convulsive Status Epilepticus. N/A