CLINICAL_TRIALS
ClinicalTrials.gov record update
Composite Adverse Events Compared Early Versus Conventional Cessation of Hydrocortisone in Patients With Septic Shock: Randomized-controlled Trial
This page presents selected fields from the linked source record. It does not add a medical interpretation.
Record identity and dates
- Source
- ClinicalTrials.gov
- Source record ID
- NCT05818826
- Title field or adapter rule
- protocolSection.identificationModule.officialTitle
- Ingested At
- 2026-04-28T10:39:51.572178+00:00
- Published At
- 2024-04-05T00:00:00+00:00
- Record Updated At
- 2024-04-05
- Timestamp Basis
- source retrieval time was not retained by the feed adapter
- Date limitation
- source retrieval time was not retained by the feed adapter
Fields recorded by this source
- protocolSection.conditionsModule.conditions
["Septic Shock", "Adverse Event", "Hydrocortisone", "Hyperglycemia", "Hypernatremia", "Muscle Weakness", "Superimposed Infection"]- protocolSection.statusModule.lastUpdatePostDateStruct.date
"2024-04-05"- protocolSection.identificationModule.nctId
"NCT05818826"- protocolSection.identificationModule.officialTitle
"Composite Adverse Events Compared Early Versus Conventional Cessation of Hydrocortisone in Patients With Septic Shock: Randomized-controlled Trial"- protocolSection.statusModule.overallStatus
"RECRUITING"- protocolSection.designModule.phases
["PHASE2"]- protocolSection.statusModule.resultsFirstPostDateStruct.date
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Study condition terms
Intervention details are not present in the imported fields for this record. No drug-condition relationship is inferred from co-listing.
This index keeps the source fields it imported; it may not contain the complete original record. Verify wording and context in the linked source.