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The assessment efficacy of electrical brain stimulation among patients with drug-resistant epilepsy

The Efficacy assessment of high definition cathodal transcranial direct current stimulation in treatment of patients with drug-resistant epilepsy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200111046082N1
Enrollment
22
Registered
2020-04-03
Start date
2018-05-05
Completion date
Unknown
Last updated
2020-04-21

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

Conditions

drug resistant epilepsy. Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, intractable

Interventions

Intervention 1: Intervention group:Patients with drug-resistant epilepsy who are not good candidates for epilepsy surgery or who do not want surgery or are waiting for surgery. In all patients, the ep

Sponsors

Kerman University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: age>=18 y/o all of patients full filled ILAE criteria of drug-resistant epilepsy participants were not good candidate for epilepsy surgery and or they will not surgery or they waited for epilepsy surgery. obtaining signed consent

Exclusion criteria

Exclusion criteria: scalp diseases(such as eczema, skin lesions) previous intracranial surgery, intracranial metal (out of mouth) such as cracking, surgical clip implanted device such as cardiac pacemaker, VNS, Cochlear implantation recurrent or severe headaches previous head trauma and other related brain diseases pregnancy and lactation

Design outcomes

Primary

MeasureTime frame
Investigating changes in the frequency of epileptic seizures. Timepoint: before intervention and monthly for 3 months. Method of measurement: seizure diary.;Investigating the frequency changes of interictal epileptiform discharges. Timepoint: immediately before and after intervention and then monthly for 3 months. Method of measurement: 30 minutes standard EEG.;Side effects. Timepoint: immediately after stimulation. Method of measurement: specialist visit.;Quality of life. Timepoint: before intervention and after 3 months. Method of measurement: full filling of the QoL in Epilepsy Inventory-89.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSoheila Rezakhani

Kerman University of Medical Sciences

drrezakhani@gmail.com+98 34 3226 3855

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026