CLINICAL_TRIALS ClinicalTrials.gov record update

A PHASE 3/4 RANDOMIZED, DOUBLE-BLIND, DOSE-RANGING STUDY OF THE SAFETY AND EFFICACY OF DEXMEDETOMIDINE (DEX) USED WITH PROPOFOL (PRO) AS NEEDED FOR PROCEDURAL SEDATION OF PEDIATRIC SUBJECTS ≥1 MONTH TO <17 YEARS OF AGE UNDERGOING MRI SCANS

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Record identity and dates

Source: ClinicalTrials.gov
Source record ID: NCT04237792
Title field or adapter rule: protocolSection.identificationModule.officialTitle
Ingested At: 2026-04-28T10:38:54.523113+00:00
Published At: 2022-11-16T00:00:00+00:00
Record Updated At: 2022-11-16
Results Posted At: 2022-11-16
Timestamp Basis: source retrieval time was not retained by the feed adapter
Date limitation: source retrieval time was not retained by the feed adapter

protocolSection.conditionsModule.conditions: ["MRI Sedation"]
protocolSection.statusModule.lastUpdatePostDateStruct.date: "2022-11-16"
protocolSection.identificationModule.nctId: "NCT04237792"
protocolSection.identificationModule.officialTitle: "A PHASE 3/4 RANDOMIZED, DOUBLE-BLIND, DOSE-RANGING STUDY OF THE SAFETY AND EFFICACY OF DEXMEDETOMIDINE (DEX) USED WITH PROPOFOL (PRO) AS NEEDED FOR PROCEDURAL SEDATION OF PEDIATRIC SUBJECTS \u22651 MONTH TO \u003c17 YEARS OF AGE UNDERGOING MRI SCANS"
protocolSection.statusModule.overallStatus: "COMPLETED"
protocolSection.designModule.phases: ["PHASE4"]
protocolSection.statusModule.resultsFirstPostDateStruct.date: "2022-11-16"

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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