CLINICAL_TRIALS
ClinicalTrials.gov record update
POST-MARKETING SURVEILLANCE TO OBSERVE SAFETY AND EFFICACY OF XYNTHA SOLOFUSE PREFILLED SYRINGE
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
- NCT03034044
- Title field or adapter rule
- protocolSection.identificationModule.officialTitle
- Ingested At
- 2026-04-28T10:39:29.379600+00:00
- Published At
- 2019-04-05T00:00:00+00:00
- Record Updated At
- 2023-11-13
- Results Posted At
- 2019-04-05
- 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
["Factor VIII Deficiency, Congenital", "Factor 8 Deficiency, Congenital", "Autosomal Hemophilia A", "Classic Hemophilia", "Hemophilia A, Congenital"]- protocolSection.statusModule.lastUpdatePostDateStruct.date
"2023-11-13"- protocolSection.identificationModule.nctId
"NCT03034044"- protocolSection.identificationModule.officialTitle
"POST-MARKETING SURVEILLANCE TO OBSERVE SAFETY AND EFFICACY OF XYNTHA SOLOFUSE PREFILLED SYRINGE"- protocolSection.statusModule.overallStatus
"COMPLETED"- protocolSection.designModule.phases
[]- protocolSection.statusModule.resultsFirstPostDateStruct.date
"2019-04-05"
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.