CLINICAL_TRIALS
ClinicalTrials.gov record update
Assessment of the Enrichment of Rare Coding Genetic Variants in Patients Affected by Neutrophil-Mediated Inflammatory Dermatoses
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
- NCT01952275
- Title field or adapter rule
- protocolSection.identificationModule.officialTitle
- Ingested At
- 2026-04-28T10:36:25.844303+00:00
- Published At
- 2016-09-27T00:00:00+00:00
- Record Updated At
- 2016-09-27
- 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
["Other Specified Inflammatory Disorders of Skin or Subcutaneous Tissue", "Pyoderma Gangrenosum", "Erosive Pustular Dermatosis of the Scalp", "Sweet\u0027s Syndrome", "Behcet\u0027s Disease", "Bowel-associated Dermatosis-arthritis Syndrome", "Pustular Psoriasis", "Acute Generalized Exanthematous Pustulosis", "Keratoderma Blenorrhagicum", "Sneddon-Wilkinson Disease", "IgA Pemphigus", "Amicrobial Pustulosis of the Folds", "Infantile Acropustulosis", "Transient Neonatal Pustulosis", "Neutrophilic Eccrine Hidradenitis", "Rheumatoid Neutrophilic Dermatitis", "Neutrophilic Urticaria", "Still\u0027s Disease", "Erythema Marginatum", "Unclassified Periodic Fever Syndromes / Autoinflammatory Syndromes", "Dermatitis Herpetiformis", "Linear IgA Bullous Dermatosis", "Bullous Systemic Lupus Erythematosus", "Inflammatory Epidermolysis Bullosa Aquisita", "Neutrophilic Dermatosis of the Dorsal Hands (Pustular Vasculitis)", "Small Vessel Vasculitis Including Urticarial Vasculitis", "Erythema Elevatum Diutinum", "Medium Vessel Vasculitis"]- protocolSection.statusModule.lastUpdatePostDateStruct.date
"2016-09-27"- protocolSection.identificationModule.nctId
"NCT01952275"- protocolSection.identificationModule.officialTitle
"Assessment of the Enrichment of Rare Coding Genetic Variants in Patients Affected by Neutrophil-Mediated Inflammatory Dermatoses"- protocolSection.statusModule.overallStatus
"UNKNOWN"- 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.