CLINICAL_TRIALS ClinicalTrials.gov record with results posted

Investigating Near-Threshold Perception During Anesthetic Sedation

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Record identity and dates

Source: ClinicalTrials.gov
Source record ID: NCT06403852
Title field or adapter rule: {'original_value': 'Investigating Near-Threshold Perception During Anesthetic Sedation', 'source_field': 'protocolSection.identificationModule.officialTitle'}
Ingested At: 2026-10-31T01:06:25.571569+00:00
Published At: 2026-10-30T00:00:00+00:00
Record Updated At: 2026-10-30
Results Posted At: 2026-10-30
Source Retrieved At: 2026-10-31T01:06:25.053101+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

protocolSection.conditionsModule.conditions: ["Propofol", "Anesthesia", "fMRI"]
protocolSection.statusModule.lastUpdatePostDateStruct: {"date": "2026-10-30", "type": "ACTUAL"}
protocolSection.identificationModule.nctId: "NCT06403852"
protocolSection.identificationModule.officialTitle: "Investigating Near-Threshold Perception During Anesthetic Sedation"
protocolSection.statusModule.overallStatus: "COMPLETED"
protocolSection.designModule.phases: ["PHASE2"]
protocolSection.statusModule.resultsFirstPostDateStruct: {"date": "2026-10-30", "type": "ACTUAL"}

{'armGroupLabels': ['Image recognition task'], 'description': 'Three 16-min sessions in wakeful baseline, light sedation, and recovery will be conducted (Fig. 2). Light sedation will be achieved by IV infusion of propofol to achieve effect-site concentrations of 1.0 μg/ml. Infusion rate will be manually controlled. An initial bolus dose (525 µg/kg) and subsequent infusion rate (82 µg/kg/min) for each participant', 'name': 'Functional Magnetic Resonance Imaging (fMRI) with propofol', 'type': 'COMBINATION_PRODUCT'} (protocolSection.armsInterventionsModule.interventions[])

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