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Trial · NCT00042224

Electroconvulsive Therapy in Clozapine Refractory Schizophrenia

NCT00042224, Phase 1, Phase 2, Completed, Northwell Health; results first posted 2015-10-15

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Electroconvulsive Therapy in Clozapine Refractory Schizophrenia. Trials, record NCT00042224. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00042224

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Electroconvulsive Therapy in Clozapine Refractory Schizophrenia
NCT number
NCT00042224
Status
Completed
Phases
Phase 1, Phase 2
Enrollment
39 participants, actual
Lead sponsor
Northwell Health
Conditions
Schizophrenia
Interventions
Electroconvulsive Therapy (ECT), Clozapine
First posted
2002-07-26
Last updated
2017-05-15
Results first posted
2015-10-15

Source ClinicalTrials.gov

Registered outcomes1

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryResponse Rates in the ECT Plus Clozapine Group vs the Pharmacotherapy Group.8 Weeks
Response is defined as 40% reduction of symptoms in the psychotic symptom sub-scale (hallucinatory behavior, suspiciousness, conceptual disorganization, and unusual thought of content) of the Brief Psychiatric Rating Scale (BPRS) at the end of the 8-week study. BPRS assesses psychotic symptoms on a 18-item scale. The severity of each item is rated on a continuous scale from 1-7, with 1 being the least severe and 7 being most severe. Participants included in the study, at baseline had at least a moderate score of 4 on one of the four psychotic symptom sub-scale or a score of 12 on all four of these items combined (ranges 4 -28, with higher scores indicative of greater severity). A reduction of symptoms would be a sub-scale score which is 40% less than participants baseline score. If a participant enters the study with a sub-scale score of 15, to be considered a responder (at least a 40% reduction in symptoms score) his/her score must decrease by at least 6 points and be 9 or less.

Outcomes1

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYResponse Rates in the ECT Plus Clozapine Group vs the Pharmacotherapy Group.8 Weeksinpatient units of the Zucker Hillside Hospital at Glen Oaks, N.Y., and the Pilgrim State Psychiatric Center in Long Island, N.Y.Percentage of respondersNUMBER

Results by group2

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Response Rates in the ECT Plus Clozapine Group vs the Pharmacotherapy Group.Electroconvulsive Therapy With Medication50Percentage of responders
Response Rates in the ECT Plus Clozapine Group vs the Pharmacotherapy Group.Medication Monotherapy0Percentage of responders

Participant flow6

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTED1 Electroconvulsive Therapy With Medication20
Overall StudySTARTED2 Medication Monotherapy19
Overall StudyCOMPLETED1 Electroconvulsive Therapy With Medication17
Overall StudyCOMPLETED2 Medication Monotherapy16
Overall StudyNOT COMPLETED1 Electroconvulsive Therapy With Medication3
Overall StudyNOT COMPLETED2 Medication Monotherapy3

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityElectroconvulsive Therapy With Medication
Total, all-cause mortalityMedication Monotherapy
Total, other adverse eventsElectroconvulsive Therapy With Medication020
Total, other adverse eventsMedication Monotherapy019
Total, serious adverse eventsElectroconvulsive Therapy With Medication020
Total, serious adverse eventsMedication Monotherapy019

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants1

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

ProjectTitlePrincipal investigatorsOrganizationFunderFiscal years
R01MH060390ECT IN CLOZAPINE REFRACTORY SCHIZOPHRENIAPETRIDES, GEORGIOSLONG ISLAND JEWISH MEDICAL CENTERNATIONAL INSTITUTE OF MENTAL HEALTH2001 to 2003

Trial comparisons1

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

Comparison
Electroconvulsive Therapy With Medication vs Medication Monotherapy: serious adverse events

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT00042224

GET https://conductscience.org/api/trials/v1/NCT00042224/registered