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Electroconvulsive Therapy in Clozapine-resistant Schizophrenia

Efficacy and Cognitive Effects of Electroconvulsive Therapy in Clozapine-Resistant Schizophrenia

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02159001
Enrollment
20
Registered
2014-06-09
Start date
2014-06-30
Completion date
2018-06-30
Last updated
2015-10-16

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

Conditions

Schizoaffective Disorder, Schizophrenia

Keywords

clozapine, ECT, PANSS, schizoaffective disorder, schizophrenia, treatment

Brief summary

Electroconvulsive therapy (ECT) is one of the oldest neuromodulation treatments still used in psychiatry. Only case reports and open label non-randomized studies have been published of ECT in clozapine-resistant schizophrenia patients. The purpose of this trial is to study the efficacy and cognitive effects of add-on ECT treatment (10-course) in schizophrenia patients taking clozapine.

Interventions

DEVICEelectroconvulsive therapy

10-course, three times a week bilateral frontotemporal ECT

Sponsors

Niuvanniemi Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 64 Years
Healthy volunteers
No

Inclusion criteria

* diagnosis of schizophrenia or schizoaffective disorder * treatment-resistant to clozapine * age 18 - 64 years * capacity and willingness to give informed consent

Exclusion criteria

* serious somatic illness * progressive neurological illness, recent brain damage or sequela of serious brain damage * ECT less than 3 months prior to this trial

Design outcomes

Primary

MeasureTime frameDescription
Positive and Negative Symptom Scale2 daysPositive and Negative Symptom Scale (PANSS) is assessed two days after ECT course

Countries

Finland

Contacts

Primary ContactEila Tiihonen, MD, PhD
eila.tiihonen@niuva.fi+358 295 242 204
Backup ContactSoile Hyvärinen, MD
soile.hyvarinen@niuva.fi+358 295 242 219

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026