Treatment of Refractory Status Epilepticus
Stopped early · Phase 3
Conditions studied: Status Epilepticus
In brief
The purpose of this study is to determine whether propofol or barbiturates should be preferred in the treatment of status epilepticus (continuous seizure activity) refractory to 2 standard antiepileptic agents.
Key facts
- Study ID
- NCT00265616
- Run by
- Brigham and Women's Hospital
- People needed
- 23
- Starts
- 2006-05-01
- Expected to finish
- 2010-03-01
- Last updated by the study team
- 2013-04-09
Who can join
Age: 16 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients with refractory status epilepticus not due to cerebral anoxia, needing coma induction for clinical management.
You may not qualify if…
- Age < 16 years old.
- Known pregnancy.
- Cerebral anoxia as SE etiology.
- Epilepsia partialis continua (simple partial SE).
- Known intolerance to the study drugs.
- Known mitochondrial disorder, hyperlipidemia, or significant rhabdomyolysis.
Where it is running
- Massachusetts General Hospital — Boston, Massachusetts, United States
- Brigham and Women's Hospital — Boston, Massachusetts, United States
- Inselspital — Bern, Canton of Bern, Switzerland
- CHUV — Lausanne, Canton of Vaud, Switzerland
- Hôpitaux Universitaires de Genève — Geneva, Switzerland
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.