Sub-Study within Project ANNOTeM (Acute Neurological care in North-East-Germany with Tele-medical Support)Effects of telemedically supported differential diagnosis and therapy of epileptic seizures – a prospective, multi-center, open-label, controlled, cluster-randomized, parallel-group study

Not Applicable

• Conditions: G40; G41; R40; Epilepsy; Status epilepticus; Somnolence, stupor and coma

• Registration Number: DRKS00013068
• Lead Sponsor: Charité Universitätsmedizin Berlin

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2017-09-26
• Study Completion: 2020-02-22
• Results First Posted: 2022-11-18
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 134

Inclusion Criteria

Patients in regional care clinics with neurological emergency syndromes such as disturbances of consciousness or epileptic seizures with or without diagnosed epilepsy.

Exclusion Criteria

non-acute syndromes (>24h),
non neurological syndromes

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
time till re-hospitalization within 6 months after study inclusion due to an epileptic seizure or loss of consciousness of unknown origin measured in days

Secondary Outcome Measures

Name	Time	Method
Frequency of seizure (predefined subgroups: Newly occurring epilepsy and pre-existing epilepsy, as well as all patients with loss of consciousness with a suspected epilept. seizure) within 6 months after the index visit;<br>Frequency of hospital admissions with similar symptoms within 6 months after the index visit;<br>AU days (days of incapacity for work) within 6 months after the index visit;<br>Change in quality of life (PROMIS-29, QOLIE 31, PESOS-2010E) between the index visit and 6 months after the index visit;