CLINICAL_TRIALS ClinicalTrials.gov record update

A Randomized, Two-Way, Single-Dose, Open-Label Study to Evaluate the Bioequivalence of a Test Tablet Formulation of Primidone 50 mg, Compared to an Equivalent Dose of Primidone (Mysoline®) in Healthy Adult Subjects

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Record identity and dates

Source: ClinicalTrials.gov
Source record ID: NCT00685165
Title field or adapter rule: protocolSection.identificationModule.officialTitle
Ingested At: 2026-04-28T10:35:00.911458+00:00
Published At: 2010-01-20T00:00:00+00:00
Record Updated At: 2010-01-20
Results Posted At: 2010-01-20
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: ["Therapeutic Equivalency"]
protocolSection.statusModule.lastUpdatePostDateStruct.date: "2010-01-20"
protocolSection.identificationModule.nctId: "NCT00685165"
protocolSection.identificationModule.officialTitle: "A Randomized, Two-Way, Single-Dose, Open-Label Study to Evaluate the Bioequivalence of a Test Tablet Formulation of Primidone 50 mg, Compared to an Equivalent Dose of Primidone (Mysoline\u00ae) in Healthy Adult Subjects"
protocolSection.statusModule.overallStatus: "COMPLETED"
protocolSection.designModule.phases: ["PHASE1"]
protocolSection.statusModule.resultsFirstPostDateStruct.date: "2010-01-20"

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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