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Observation of CBD therapy inpatients with intractable epilepsy

Observation of CBD therapy inpatients with intractable epilepsy - CBD-ET

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
DRKS
Registry ID
DRKS00013177
Enrollment
40
Registered
2019-06-25
Start date
2017-12-01
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

Interventions

Group 1: Cannabidiol oily solution start 5mg/kg/d, up titrated according to tolerance to maximum of 50mg/kg/d.

Sponsors

Abteilung für Epileptologie des Universitätsklinikums Freiburg
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Months to No maximum

Inclusion criteria

Inclusion criteria: pharmacoresistant epilepsy, treatment with at least one anticonvulsive drug, CBD therapy

Exclusion criteria

Exclusion criteria: cannabinoid treatment within 4 weeks of screening, pregnancy, instable hepatic or renal disease

Design outcomes

Primary

MeasureTime frame
Percentage change of seizure frequency per month of motor seizures after 3 months of CBD compared to 1 month of baseline

Secondary

MeasureTime frame
Percentage change of seizure frequency per month of all seizures after 3 months of CBD compared to 1 month of baseline plus change of motor and all seizures per month after 6,12,18,24,36 months of treatment compared to baseline

Countries

Germany

Contacts

Public ContactKerstin Alexandra Klotz

Abteilung für Epileptologie des Universitätsklinikums Freiburg

kerstin.alexandra.klotz@uniklinik-freiburg.de+4976127043520

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 20, 2026