Management of Non Convulsive Status Epilepticus
1 other identifier
observational
100
1 country
1
Brief Summary
Non convulsive status epilepticus is a persistent change in behavioural and or mental process from baseline associated with continuous epileptiform activity in electroencephalograph,it occur in about 50 percent in patients with coma and convulsions and in 8-13 percent in intensive care unit patients
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Dec 2017
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 4, 2017
CompletedFirst Posted
Study publicly available on registry
August 10, 2017
CompletedStudy Start
First participant enrolled
December 1, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
April 1, 2019
CompletedAugust 10, 2017
August 1, 2017
1 year
August 4, 2017
August 7, 2017
Conditions
Outcome Measures
Primary Outcomes (1)
Number of cured patients
Number of cured patients
An average of 1 year
Interventions
Electroencephalograph will be done to all patients who fulfill the inclusion criteria to detect presence of electrical discharge with in the brain.Complete blood count ,liver function test ,kidney function test ,blood glucose level and serum electrolytes will be done to selected cases according to the clinical presentation
Eligibility Criteria
* Patients 1-18 years * Generalized tonic clonic convulsions and prolonged post ictal period more than 30 minutes * Un explained coma ,stupor,confusion and psychic or speech disorder
You may qualify if:
- patients who have generalized tonic colonic convulsions and prolonged post ictal state more than 30 minutes
- patients presented with un explained psychic or speech disorder
- patients presented with stupor or confusion
- Patients presented with un explained coma
You may not qualify if:
- patients with progressive neurological disease
- Patients with severe cerebral anoxia
- Patients with liver or hepatic impairment
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
AssiutU
Asyut, Egypt
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Rewaa Mohammed, MD
Assiut University
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principlal investigator
Study Record Dates
First Submitted
August 4, 2017
First Posted
August 10, 2017
Study Start
December 1, 2017
Primary Completion
December 1, 2018
Study Completion
April 1, 2019
Last Updated
August 10, 2017
Record last verified: 2017-08