CLINICAL_TRIALS
ClinicalTrials.gov record update
WiTNNess: An International Natural History Study of Autosomal Recessive TNNT1 Myopathy
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
- NCT06374719
- Title field or adapter rule
- protocolSection.identificationModule.officialTitle
- Ingested At
- 2026-04-25T22:26:51.798401+00:00
- Published At
- 2025-02-12T00:00:00+00:00
- Record Updated At
- 2025-02-12
- 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
["TNNT1-associated Myopathy", "Infantile-onset Nemaline Rod Myopathy", "Myopathies, Nemaline", "Myopathy", "Myopathy, Rod", "Myopathy; Hereditary", "Amish Nemaline Myopathy", "Nemaline Myopathy 5", "NEM5", "Genetic Muscle Disease", "Recessive Hereditary Disorder (Autosomal)", "ANM"]- protocolSection.statusModule.lastUpdatePostDateStruct.date
"2025-02-12"- protocolSection.identificationModule.nctId
"NCT06374719"- protocolSection.identificationModule.officialTitle
"WiTNNess: An International Natural History Study of Autosomal Recessive TNNT1 Myopathy"- protocolSection.statusModule.overallStatus
"RECRUITING"- protocolSection.designModule.phases
[]- 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.