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CLINICAL_TRIALS ClinicalTrials.gov record update

A 50-Week Prospective, Double-Blinded, Randomized, Cross-over Design in Multicenter Study of100 Unit of Abobotulinum Toxin Type A (Dysport®) Versus 33.33 Unit of Neubotulinum Toxin Type A (Neuronox®) Injection for Hemifacial Spasm in Thai Patients

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT04589364
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-25T22:26:34.931885+00:00
Published At
2024-04-26T00:00:00+00:00
Record Updated At
2024-04-26
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
["Hemifacial Spasm"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2024-04-26"
protocolSection.identificationModule.nctId
"NCT04589364"
protocolSection.identificationModule.officialTitle
"A 50-Week Prospective, Double-Blinded, Randomized, Cross-over Design in Multicenter Study of100 Unit of Abobotulinum Toxin Type A (Dysport\u00ae) Versus 33.33 Unit of Neubotulinum Toxin Type A (Neuronox\u00ae) Injection for Hemifacial Spasm in Thai Patients"
protocolSection.statusModule.overallStatus
"NOT_YET_RECRUITING"
protocolSection.designModule.phases
["PHASE3"]
protocolSection.statusModule.resultsFirstPostDateStruct.date
""

Study condition terms

  • Hemifacial Spasm (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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