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

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 - ANNOTeM-EPI

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00013068

Enrollment

800

Registered

2017-09-26

Start date

2017-11-29

Completion date

Unknown

Last updated

2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

G40 G41 R40

Interventions

Group 1: A with tele-epilepsy consultation: Within 48 hours after an acute hospital admission due to an epileptic seizure or unconsciousness of unknown origin, the patients are advised individually

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

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

Exclusion criteria: non-acute syndromes (>24h), non neurological syndromes

Design outcomes

Primary

Measure	Time frame
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

Measure	Time frame
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; Frequency of hospital admissions with similar symptoms within 6 months after the index visit; AU days (days of incapacity for work) within 6 months after the index visit; Change in quality of life (PROMIS-29, QOLIE 31, PESOS-2010E) between the index visit and 6 months after the index visit;	—

Measure

Time frame

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; Frequency of hospital admissions with similar symptoms within 6 months after the index visit; AU days (days of incapacity for work) within 6 months after the index visit; Change in quality of life (PROMIS-29, QOLIE 31, PESOS-2010E) between the index visit and 6 months after the index visit;

—

Countries

Germany

Contacts

Public ContactJoachim Weber

Charité Universitätsmedizin Berlin

joachim.weber@charite.de+49 30450543524

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 17, 2026