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NCT03562351

Seizure Rescue Medication: Caregiver Education in a Simulation Setting

Completed NA Last updated 4 September 2020
What this trial tests

NA trial testing Verbal Instructions Educational Intervention in Status Epilepticus in 17 participants. Completed in 17 September 2019.

Timeline
1 July 2018
Primary endpoint
17 September 2019
17 September 2019

Quick facts

Lead sponsorBoston Children's Hospital
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposeprevention
Enrollment17
Start date1 July 2018
Primary completion17 September 2019
Estimated completion17 September 2019
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Boston Children's Hospital

Who can join

Adults 2 to 80, any sex, with Status Epilepticus. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

1\. Design an educational quality improvement program to assess the most effective educational approach on caregiver seizure RM application. The investigators hypothesize that this educational program will improve caregiver comfort, knowledge of emergent seizure care, and time to medication application. Specifically, the aims include: 1. Create an educational video reviewing RM administration 2. Develop and validate a simulation training model/mannequin for rectal diazepam administration 3. Expand training to other seizure RMs (e.g. intranasal midazolam, buccal lorazepam) and transition the most effective educational model back to the clinics/bedside to standardize caregiver teaching throughout the department/hospital

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Status Epilepticus

Currently open trials in the same condition.

Other Boston Children's Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing