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CLINICAL_TRIALS ClinicalTrials.gov record update

Determination of Safety and Effectiveness of the SilverHawk™ Peripheral Plaque Excision System for Calcium (SilverHawk LS-C) and the SpiderFX™ Embolic Protection Device for the Treatment of Calcified Peripheral Arterial Disease in the Superficial Femoral and/or the Popliteal Arteries (DEFINITIVE Ca++)

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT00733135
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-28T10:35:51.190881+00:00
Published At
2014-07-04T00:00:00+00:00
Record Updated At
2015-08-26
Results Posted At
2014-07-04
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
["Peripheral Arterial Disease"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2015-08-26"
protocolSection.identificationModule.nctId
"NCT00733135"
protocolSection.identificationModule.officialTitle
"Determination of Safety and Effectiveness of the SilverHawk\u2122 Peripheral Plaque Excision System for Calcium (SilverHawk LS-C) and the SpiderFX\u2122 Embolic Protection Device for the Treatment of Calcified Peripheral Arterial Disease in the Superficial Femoral and/or the Popliteal Arteries (DEFINITIVE Ca++)"
protocolSection.statusModule.overallStatus
"COMPLETED"
protocolSection.designModule.phases
["PHASE2", "PHASE3"]
protocolSection.statusModule.resultsFirstPostDateStruct.date
"2014-07-04"

Study condition terms

  • Peripheral Arterial Disease (protocolSection.conditionsModule.conditions)

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.