NCT03245099

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

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
100

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Dec 2017

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

August 4, 2017

Completed
6 days until next milestone

First Posted

Study publicly available on registry

August 10, 2017

Completed
4 months until next milestone

Study Start

First participant enrolled

December 1, 2017

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2018

Completed
4 months until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2019

Completed
Last Updated

August 10, 2017

Status Verified

August 1, 2017

Enrollment Period

1 year

First QC Date

August 4, 2017

Last Update Submit

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

Age12 Months - 18 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64)
Sampling MethodNon-Probability Sample
Study Population

* 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

Location

MeSH Terms

Conditions

Status Epilepticus

Interventions

Cross-Sectional Studies

Condition Hierarchy (Ancestors)

SeizuresNeurologic ManifestationsNervous System DiseasesSigns and SymptomsPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Epidemiologic StudiesEpidemiologic Study CharacteristicsEpidemiologic MethodsInvestigative TechniquesHealth Care Evaluation MechanismsQuality of Health CareHealth Care Quality, Access, and EvaluationPublic HealthEnvironment and Public Health

Study Officials

  • Rewaa Mohammed, MD

    Assiut University

    PRINCIPAL INVESTIGATOR

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

Locations