CLINICAL_TRIALS
ClinicalTrials.gov record update
Postoperative Sore Throat in Children: Comparison Between Two Supraglottic Devices, Ambu® AuraOnce™ Laryngeal Mask Airway (LMA) and I-Gel® in Children Undergoing Elective Lower Abdominal or Orthopedic Surgery.
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
- NCT03140228
- Title field or adapter rule
- protocolSection.identificationModule.officialTitle
- Ingested At
- 2026-04-28T10:37:12.942602+00:00
- Published At
- 2019-08-02T00:00:00+00:00
- Record Updated At
- 2019-08-02
- 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
["Laryngeal Masks", "Pharyngitis", "Minors", "Anesthesia"]- protocolSection.statusModule.lastUpdatePostDateStruct.date
"2019-08-02"- protocolSection.identificationModule.nctId
"NCT03140228"- protocolSection.identificationModule.officialTitle
"Postoperative Sore Throat in Children: Comparison Between Two Supraglottic Devices, Ambu\u00ae AuraOnce\u2122 Laryngeal Mask Airway (LMA) and I-Gel\u00ae in Children Undergoing Elective Lower Abdominal or Orthopedic Surgery."- protocolSection.statusModule.overallStatus
"COMPLETED"- protocolSection.designModule.phases
["NA"]- protocolSection.statusModule.resultsFirstPostDateStruct.date
""
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.