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Trial · NCT01526395

Decreasing the Use of Unmodified Electroconvulsive Therapy (ECT) in an Indian Hospital

NCT01526395, Not applicable, Completed, Johns Hopkins University

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Decreasing the Use of Unmodified Electroconvulsive Therapy (ECT) in an Indian Hospital. Trials, record NCT01526395. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT01526395

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Trial

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

Title
Decreasing the Use of Unmodified Electroconvulsive Therapy (ECT) in an Indian Hospital
NCT number
NCT01526395
Status
Completed
Phases
Not applicable
Enrollment
99 participants, actual
Lead sponsor
Johns Hopkins University
Conditions
Major Depressive Disorder, Bipolar Disorder, Schizophrenia
Interventions
Propofol
First posted
2012-02-03
Last updated
2013-04-04

Source ClinicalTrials.gov

Registered outcomes9

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

ListOutcomeTime frameDescription
PrimaryPercentage of patients receiving ECT who agree to the modified form of treatment after it is offered.6 months
SecondaryRate at which ECT is offered and refused.6 months
SecondaryChange in patient anxiety measured by the state portion of the State-Trait Anxiety Inventory.Baseline and completion of ECT treatments or up to 6 months, whichever comes first
SecondaryInpatient length of stay calculated from onset of ECT administration.6 months
SecondaryNumber of ECTs required to complete a course of treatment6 months
Secondary
Changes in scales used to assess severity of symptoms. The investigators will record changes in the Hamilton Depression Rating Scale, the Young Mania Rating Scale, the Brief Psychiatric Rating Scale and the Clinical Global Impression Severity scale.
Baseline and completion of ECT treatments or up to 6 months, whichever comes first
SecondaryCognitive changes, monitored by the Mini Mental State Examination (MMSE)Baseline and completion of ECT treatments or up to 6 months, whichever comes first
SecondaryMonitoring of adverse effects such the occurence of emergent delirium, headaches, muscle aches, nausea and vomiting, and fractures and dislocations.Baseline and completion of ECT treatments or up to 6 months, whichever comes first
SecondaryMonitoring of delirium using the test with the Confusion Assessment Method for the ICU (CAM-ICU).Baseline and completion of ECT treatments or up to 6 months, whichever comes first

Outcomes0

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

None in this release.

Results by group0

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

None in this release.

Participant flow0

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

None in this release.

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 totals0

The totals the trial posted for each group.

None in this release.

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants0

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.

None in this release.

Trial comparisons0

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

None in this release.

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/NCT01526395

GET https://conductscience.org/api/trials/v1/NCT01526395/registered