Catalyst Wire Dossier Catalyst Wire Dossier
CLINICAL_TRIALS ClinicalTrials.gov record update

Post-Market Clinical Follow-up Registry of Patients With CODMAN CERTAS Plus Programmable Valves

This page presents selected fields from the linked source record. It does not add a medical interpretation.

Open original source record ↗

Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT04207229
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-28T10:38:19.975225+00:00
Published At
2022-01-26T00:00:00+00:00
Record Updated At
2022-01-26
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
["Hydrocephalus", "NPH (Normal Pressure Hydrocephalus)", "IIH - Idiopathic Intracranial Hypertension"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2022-01-26"
protocolSection.identificationModule.nctId
"NCT04207229"
protocolSection.identificationModule.officialTitle
"Post-Market Clinical Follow-up Registry of Patients With CODMAN CERTAS Plus Programmable Valves"
protocolSection.statusModule.overallStatus
"COMPLETED"
protocolSection.designModule.phases
[]
protocolSection.statusModule.resultsFirstPostDateStruct.date
""

Study condition terms

  • Hydrocephalus (protocolSection.conditionsModule.conditions)
  • NPH (Normal Pressure Hydrocephalus) (protocolSection.conditionsModule.conditions)
  • IIH - Idiopathic Intracranial Hypertension (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.