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Persona® OsseoTi® Keel Compatibility Study-A Multicenter Cohort Study A Prospective, Post-market Clinical Follow-up Study to Demonstrate Safety, Performance and Clinical Benefits of the Persona Knee System Portfolio and Its Instrumentation

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT05787821
Title field or adapter rule
{'original_value': 'Persona® OsseoTi® Keel Compatibility Study-A Multicenter Cohort Study A Prospective, Post-market Clinical Follow-up Study to Demonstrate Safety, Performance and Clinical Benefits of the Persona Knee System Portfolio and Its Instrumentation', 'source_field': 'protocolSection.identificationModule.officialTitle'}
Ingested At
2026-10-31T23:27:34.159150+00:00
Published At
2026-10-19T00:00:00+00:00
Record Updated At
2026-10-19
Source Retrieved At
2026-10-31T22:18:41.628690+00:00
Timestamp Basis
ClinicalTrials.gov API/RSS response retrieval timestamp recorded by Dossier adapter
Date limitation
ClinicalTrials.gov API/RSS response retrieval timestamp recorded by Dossier adapter

Fields recorded by this source

protocolSection.conditionsModule.conditions
["Knee Pain Chronic", "Osteoarthritis, Knee", "Rheumatoid Arthritis", "Traumatic Arthritis", "Polyarthritis", "Varus Deformity", "Valgus Deformity", "Flexion Deformity of Knee", "Avascular Necrosis"]
protocolSection.statusModule.lastUpdatePostDateStruct
{"date": "2026-10-19", "type": "ACTUAL"}
protocolSection.identificationModule.nctId
"NCT05787821"
protocolSection.identificationModule.officialTitle
"Persona\u00ae OsseoTi\u00ae Keel Compatibility Study-A Multicenter Cohort Study A Prospective, Post-market Clinical Follow-up Study to Demonstrate Safety, Performance and Clinical Benefits of the Persona Knee System Portfolio and Its Instrumentation"
protocolSection.statusModule.overallStatus
"ACTIVE_NOT_RECRUITING"
protocolSection.designModule.phases
null
protocolSection.statusModule.resultsFirstPostDateStruct
null

Study condition terms

  • Knee Pain Chronic (protocolSection.conditionsModule.conditions)
  • Osteoarthritis, Knee (protocolSection.conditionsModule.conditions)
  • Rheumatoid Arthritis (protocolSection.conditionsModule.conditions)
  • Traumatic Arthritis (protocolSection.conditionsModule.conditions)
  • Polyarthritis (protocolSection.conditionsModule.conditions)
  • Varus Deformity (protocolSection.conditionsModule.conditions)
  • Valgus Deformity (protocolSection.conditionsModule.conditions)
  • Flexion Deformity of Knee (protocolSection.conditionsModule.conditions)
  • Avascular Necrosis (protocolSection.conditionsModule.conditions)

Interventions recorded in this study

  • {'armGroupLabels': ['Cohort 1', 'Cohort 10', 'Cohort 11', 'Cohort 12', 'Cohort 2', 'Cohort 3', 'Cohort 4', 'Cohort 5', 'Cohort 6', 'Cohort 7', 'Cohort 8', 'Cohort 9'], 'description': 'Total knee replacement.', 'name': 'Total Knee Arthroplasty', 'type': 'DEVICE'} (protocolSection.armsInterventionsModule.interventions[])

An intervention appearing in a study record does not establish an effect or an approved use.

This index keeps the source fields it imported; it may not contain the complete original record. Verify wording and context in the linked source.