Randomized Controlled Trial Comparing the Impact of Patient Education Strategies on the Antidepressant Response to Propofol Sedation

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Record identity and dates

Source

ClinicalTrials.gov

Source record ID

NCT06705270

Title field or adapter rule

{'original_value': 'Randomized Controlled Trial Comparing the Impact of Patient Education Strategies on the Antidepressant Response to Propofol Sedation', 'source_field': 'protocolSection.identificationModule.officialTitle'}

Ingested At

2026-10-31T23:27:37.357984+00:00

Published At

2026-10-27T00:00:00+00:00

Record Updated At

2026-10-27

Source Retrieved At

2026-10-31T22:19:07.580396+00:00

Timestamp Basis

ClinicalTrials.gov API/RSS response retrieval timestamp recorded by Dossier adapter

Date limitation

ClinicalTrials.gov API/RSS response retrieval timestamp recorded by Dossier adapter

Fields recorded by this source

protocolSection.conditionsModule.conditions

["Major Depressive Disorder (MDD)"]

protocolSection.statusModule.lastUpdatePostDateStruct

{"date": "2026-10-27", "type": "ACTUAL"}

protocolSection.identificationModule.nctId

"NCT06705270"

protocolSection.identificationModule.officialTitle

"Randomized Controlled Trial Comparing the Impact of Patient Education Strategies on the Antidepressant Response to Propofol Sedation"

protocolSection.statusModule.overallStatus

"NOT_YET_RECRUITING"

protocolSection.designModule.phases

["NA"]

protocolSection.statusModule.resultsFirstPostDateStruct

null

Study condition terms

• Major Depressive Disorder (MDD) (protocolSection.conditionsModule.conditions)

Interventions recorded in this study

• {'armGroupLabels': ['Part 1: Response-focused education'], 'description': 'Once participants recover from sedation, they will receive education that is focused on their response to treatment.', 'name': 'Response-focused education', 'type': 'BEHAVIORAL'} (protocolSection.armsInterventionsModule.interventions[])
• {'armGroupLabels': ['Part 1: Diagnosis-focused education'], 'description': 'Once participants recover from sedation, they will be provided education that is focused on their diagnosis of major depressive disorder.', 'name': 'Diagnosis-focused education', 'type': 'BEHAVIORAL'} (protocolSection.armsInterventionsModule.interventions[])
• {'armGroupLabels': ['Part 2: IV naloxone during education'], 'description': 'A single dose of IV naloxone given during the educational intervention.', 'name': 'IV naloxone', 'type': 'DRUG'} (protocolSection.armsInterventionsModule.interventions[])
• {'armGroupLabels': ['Part 2: IV saline during education'], 'description': 'A single dose of IV saline given during the educational intervention.', 'name': 'IV saline', 'type': 'DRUG'} (protocolSection.armsInterventionsModule.interventions[])

An intervention appearing in a study record does not establish an effect or an approved use.

Drug names recorded in this source

• IV naloxone (protocolSection.armsInterventionsModule.interventions[].name)
• IV saline (protocolSection.armsInterventionsModule.interventions[].name)

A recorded drug name is not by itself an indication or a condition-specific relationship.

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