Catalyst Wire Dossier Catalyst Wire Dossier
CLINICAL_TRIALS ClinicalTrials.gov record with results posted

SMART Trial to Predict Anhedonia Response to Antidepressant Treatment

This page presents selected fields from the linked source record. It does not add a medical interpretation.

Open original source record ↗

Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT05537584
Title field or adapter rule
{'original_value': 'SMART Trial to Predict Anhedonia Response to Antidepressant Treatment', 'source_field': 'protocolSection.identificationModule.officialTitle'}
Ingested At
2026-10-31T01:06:25.673085+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

Fields recorded by this source

protocolSection.conditionsModule.conditions
["Major Depressive Disorder"]
protocolSection.statusModule.lastUpdatePostDateStruct
{"date": "2026-10-30", "type": "ACTUAL"}
protocolSection.identificationModule.nctId
"NCT05537584"
protocolSection.identificationModule.officialTitle
"SMART Trial to Predict Anhedonia Response to Antidepressant Treatment"
protocolSection.statusModule.overallStatus
"COMPLETED"
protocolSection.designModule.phases
["PHASE4"]
protocolSection.statusModule.resultsFirstPostDateStruct
{"date": "2026-10-30", "type": "ACTUAL"}

Study condition terms

  • Major Depressive Disorder (protocolSection.conditionsModule.conditions)

Interventions recorded in this study

  • {'armGroupLabels': ['MDD with BUP+ Response Marker', 'MDD with SERT+ Response Marker'], 'description': 'Subjects will receive 8 weeks of sertraline while monitored by the study physician', 'name': 'Sertraline', 'type': 'DRUG'} (protocolSection.armsInterventionsModule.interventions[])
  • {'armGroupLabels': ['MDD with BUP+ Response Marker', 'MDD with SERT+ Response Marker'], 'description': 'Subjects will receive 8 weeks of bupropion while monitored by the study physician', 'name': 'Bupropion', '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

  • Sertraline (protocolSection.armsInterventionsModule.interventions[].name)
  • Bupropion (protocolSection.armsInterventionsModule.interventions[].name)

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

This index keeps the source fields it imported; it may not contain the complete original record. Verify wording and context in the linked source.