CLINICAL_TRIALS
ClinicalTrials.gov record update
Definition of the Genotype and Clinical Phenotype of Primary Pigmented Nodular Adrenocortical Disease (PPNAD), Carney Complex, Peutz-Jeghers Syndrome and Related Conditions
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
- NCT00001452
- Title field or adapter rule
- protocolSection.identificationModule.officialTitle
- Ingested At
- 2026-04-25T22:28:07.987984+00:00
- Published At
- 2026-03-27T00:00:00+00:00
- Record Updated At
- 2026-03-27
- 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
["Cushing\u0027s Syndrome", "Pituitary Adenoma", "Carney Complex", "Primary Pigmented Nodular Adrenocortical Disease", "Peutz-Jeghers Syndrome"]- protocolSection.statusModule.lastUpdatePostDateStruct.date
"2026-03-27"- protocolSection.identificationModule.nctId
"NCT00001452"- protocolSection.identificationModule.officialTitle
"Definition of the Genotype and Clinical Phenotype of Primary Pigmented Nodular Adrenocortical Disease (PPNAD), Carney Complex, Peutz-Jeghers Syndrome and Related Conditions"- protocolSection.statusModule.overallStatus
"COMPLETED"- 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.