CLINICAL_TRIALS
ClinicalTrials.gov record update
Multi-Center Acute Safety Trial of TactiCath™ Contact Force Ablation Catheter, Sensor Enabled™ (TactiCath SE) for the Treatment of Drug Refractory Recurrent Symptomatic Paroxysmal Atrial Fibrillation
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
- NCT03354663
- Title field or adapter rule
- protocolSection.identificationModule.officialTitle
- Ingested At
- 2026-04-28T10:39:32.280278+00:00
- Published At
- 2019-08-20T00:00:00+00:00
- Record Updated At
- 2023-10-11
- Results Posted At
- 2019-08-20
- Timestamp Basis
- source retrieval time was not retained by the feed adapter
- Date limitation
- source retrieval time was not retained by the feed adapter
Fields recorded by this source
- protocolSection.conditionsModule.conditions
["Paroxysmal Atrial Fibrillation"]- protocolSection.statusModule.lastUpdatePostDateStruct.date
"2023-10-11"- protocolSection.identificationModule.nctId
"NCT03354663"- protocolSection.identificationModule.officialTitle
"Multi-Center Acute Safety Trial of TactiCath\u2122 Contact Force Ablation Catheter, Sensor Enabled\u2122 (TactiCath SE) for the Treatment of Drug Refractory Recurrent Symptomatic Paroxysmal Atrial Fibrillation"- protocolSection.statusModule.overallStatus
"COMPLETED"- protocolSection.designModule.phases
["NA"]- protocolSection.statusModule.resultsFirstPostDateStruct.date
"2019-08-20"
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.