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CLINICAL_TRIALS ClinicalTrials.gov record update

A Prospective, Non-randomized, Two Arm, Multi-center Clinical Trial to Evaluate the Safety and Efficacy of the Absolute Pro™ Peripheral Self-Expanding Stent System and the Omnilink Elite™ Peripheral Balloon-Expandable Stent System in Subjects With Atherosclerotic de Novo or Restenotic Lesions in the Native Common Iliac Artery and/or Native External Iliac Artery.

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT01396525
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-28T10:36:00.524153+00:00
Published At
2012-10-01T00:00:00+00:00
Record Updated At
2016-02-08
Results Posted At
2012-10-01
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 Vascular Disease"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2016-02-08"
protocolSection.identificationModule.nctId
"NCT01396525"
protocolSection.identificationModule.officialTitle
"A Prospective, Non-randomized, Two Arm, Multi-center Clinical Trial to Evaluate the Safety and Efficacy of the Absolute Pro\u2122 Peripheral Self-Expanding Stent System and the Omnilink Elite\u2122 Peripheral Balloon-Expandable Stent System in Subjects With Atherosclerotic de Novo or Restenotic Lesions in the Native Common Iliac Artery and/or Native External Iliac Artery."
protocolSection.statusModule.overallStatus
"COMPLETED"
protocolSection.designModule.phases
["PHASE3"]
protocolSection.statusModule.resultsFirstPostDateStruct.date
"2012-10-01"

Study condition terms

  • Peripheral Vascular 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.

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