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Treat Clozapine ( CLZ )-Resistant Schizophrenia Comparing CLZ + Haloperidol vs. CLZ + Electroconvulsive Therapy (ECT)

Treatment of Clozapine-resistant Schizophrenia : Comparison Between Augmentation With Haloperidol and Electroconvulsive Therapy

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00753051
Acronym
TCRS
Enrollment
18
Registered
2008-09-16
Start date
2008-06-30
Completion date
2012-05-31
Last updated
2012-05-07

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

Conditions

Schizophrenia

Keywords

clozapine-resistant schizophrenics, haloperidol augmenting clozapine, electroconvulsive therapy augmenting clozapine

Brief summary

Clozapine treatment resistant schizophrenia is still prevalent.The effectiveness of augmenting clozapine : one augmenting with haloperidol and the other with electroconvulsive therapy should be determined.This study is a randomized control trial.

Interventions

DRUGclozapine+haloperidol

clozapine 300-900 mg/d haloperidol 4-60 mg/d

DRUGclozapine,electroconvulsive therapy

clozapine 300-900 mg/d electroconvulsive therapy 4-12 times

Sponsors

Khon Kaen University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

1. schizophrenic patients diagnosed with schedules for clinical assessment in neuropsychiatry ( SCAN )in accordance with DSM-IV-TR or ICD-10 2. Resistant to at least 6 weeks of clozapine treatment in therapeutic dosage 3. Voluntary to participate the research protocol expressed by signing informed consent form

Exclusion criteria

1. Patient does not volunteer himself or herself 2. Patient is having epilepsy, DM, cardiac disease, autistic disorder and illiterate 3. Patient is deaf, blind , dumb to obstruct good communication

Design outcomes

Primary

MeasureTime frame
PANSS , HAM-D , CGI , AIMS Scoresevery 4 weeks for 24 weeks

Countries

Thailand

Outcome results

None listed

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