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CLINICAL_TRIALS ClinicalTrials.gov record update

A Phase 4 Randomized, Double-blind Study Comparing Patient Comfort and Safety Between Iodixanol 320 mg I/mL and Iopamidol 370 mg I/mL in Patients Undergoing Contrast-Enhanced Computed Tomographic (CECT) Imaging of the Abdomen/Pelvis

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT01376089
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-28T10:35:35.124985+00:00
Published At
2013-12-19T00:00:00+00:00
Record Updated At
2013-12-19
Results Posted At
2013-12-19
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
["Patient Comfort and Safety"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2013-12-19"
protocolSection.identificationModule.nctId
"NCT01376089"
protocolSection.identificationModule.officialTitle
"A Phase 4 Randomized, Double-blind Study Comparing Patient Comfort and Safety Between Iodixanol 320 mg I/mL and Iopamidol 370 mg I/mL in Patients Undergoing Contrast-Enhanced Computed Tomographic (CECT) Imaging of the Abdomen/Pelvis"
protocolSection.statusModule.overallStatus
"COMPLETED"
protocolSection.designModule.phases
["PHASE4"]
protocolSection.statusModule.resultsFirstPostDateStruct.date
"2013-12-19"

Study condition terms

  • Patient Comfort and Safety (protocolSection.conditionsModule.conditions)

Intervention details are not present in the imported fields for this record. No drug-condition relationship is inferred from co-listing.

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