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Familial Investigations of Childhood Cancer Predisposition

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT03050268
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-25T22:29:03.790807+00:00
Published At
2026-04-23T00:00:00+00:00
Record Updated At
2026-04-23
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
["Acute Leukemia", "Adenomatous Polyposis", "Adrenocortical Carcinoma", "AML", "BAP1 Tumor Predisposition Syndrome", "Carney Complex", "Choroid Plexus Carcinoma", "Constitutional Mismatch Repair Deficiency Syndrome", "Diamond-Blackfan Anemia", "DICER1 Syndrome", "Dyskeratosis Congenita", "Emberger Syndrome", "Familial Acute Myeloid Leukemia", "Familial Adenomatous Polyposis", "Fanconi Anemia", "Familial Cancer", "Familial Wilms Tumor", "Familial Neuroblastoma", "GIST", "Hereditary Breast and Ovarian Cancer", "Hereditary Paraganglioma-Pheochromocytoma Syndrome", "Hodgkin Lymphoma", "Juvenile Polyposis", "Li-Fraumeni Syndrome", "Lynch Syndrome", "MDS", "Melanoma Syndrome", "Multiple Endocrine Neoplasia Type 1", "Multiple Endocrine Neoplasia Type 2", "Neuroblastoma", "Neurofibromatosis Type 1", "Neurofibromatosis Type II", "Nevoid Basal Cell Carcinoma Syndrome", "Non Hodgkin Lymphoma", "Noonan Syndrome and Other Rasopathy", "Overgrowth Syndromes", "Pancreatic Cancer", "Peutz-Jeghers Syndrome", "Pheochromocytoma/Paraganglioma", "PTEN Hamartoma Tumor Syndrome", "Retinoblastoma", "Rhabdoid Tumor Predisposition Syndrome", "Rhabdomyosarcoma", "Rothmund-Thomson Syndrome", "Tuberous Sclerosis", "Von Hippel-Lindau Disease"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2026-04-23"
protocolSection.identificationModule.nctId
"NCT03050268"
protocolSection.identificationModule.officialTitle
"Familial Investigations of Childhood Cancer Predisposition"
protocolSection.statusModule.overallStatus
"RECRUITING"
protocolSection.designModule.phases
[]
protocolSection.statusModule.resultsFirstPostDateStruct.date
""

Study condition terms

  • Acute Leukemia (protocolSection.conditionsModule.conditions)
  • Adenomatous Polyposis (protocolSection.conditionsModule.conditions)
  • Adrenocortical Carcinoma (protocolSection.conditionsModule.conditions)
  • AML (protocolSection.conditionsModule.conditions)
  • BAP1 Tumor Predisposition Syndrome (protocolSection.conditionsModule.conditions)
  • Carney Complex (protocolSection.conditionsModule.conditions)
  • Choroid Plexus Carcinoma (protocolSection.conditionsModule.conditions)
  • Constitutional Mismatch Repair Deficiency Syndrome (protocolSection.conditionsModule.conditions)
  • Diamond-Blackfan Anemia (protocolSection.conditionsModule.conditions)
  • DICER1 Syndrome (protocolSection.conditionsModule.conditions)
  • Dyskeratosis Congenita (protocolSection.conditionsModule.conditions)
  • Emberger Syndrome (protocolSection.conditionsModule.conditions)
  • Familial Acute Myeloid Leukemia (protocolSection.conditionsModule.conditions)
  • Familial Adenomatous Polyposis (protocolSection.conditionsModule.conditions)
  • Fanconi Anemia (protocolSection.conditionsModule.conditions)
  • Familial Cancer (protocolSection.conditionsModule.conditions)
  • Familial Wilms Tumor (protocolSection.conditionsModule.conditions)
  • Familial Neuroblastoma (protocolSection.conditionsModule.conditions)
  • GIST (protocolSection.conditionsModule.conditions)
  • Hereditary Breast and Ovarian Cancer (protocolSection.conditionsModule.conditions)
  • Hereditary Paraganglioma-Pheochromocytoma Syndrome (protocolSection.conditionsModule.conditions)
  • Hodgkin Lymphoma (protocolSection.conditionsModule.conditions)
  • Juvenile Polyposis (protocolSection.conditionsModule.conditions)
  • Li-Fraumeni Syndrome (protocolSection.conditionsModule.conditions)
  • Lynch Syndrome (protocolSection.conditionsModule.conditions)
  • MDS (protocolSection.conditionsModule.conditions)
  • Melanoma Syndrome (protocolSection.conditionsModule.conditions)
  • Multiple Endocrine Neoplasia Type 1 (protocolSection.conditionsModule.conditions)
  • Multiple Endocrine Neoplasia Type 2 (protocolSection.conditionsModule.conditions)
  • Neuroblastoma (protocolSection.conditionsModule.conditions)
  • Neurofibromatosis Type 1 (protocolSection.conditionsModule.conditions)
  • Neurofibromatosis Type II (protocolSection.conditionsModule.conditions)
  • Nevoid Basal Cell Carcinoma Syndrome (protocolSection.conditionsModule.conditions)
  • Non Hodgkin Lymphoma (protocolSection.conditionsModule.conditions)
  • Noonan Syndrome and Other Rasopathy (protocolSection.conditionsModule.conditions)
  • Overgrowth Syndromes (protocolSection.conditionsModule.conditions)
  • Pancreatic Cancer (protocolSection.conditionsModule.conditions)
  • Peutz-Jeghers Syndrome (protocolSection.conditionsModule.conditions)
  • Pheochromocytoma/Paraganglioma (protocolSection.conditionsModule.conditions)
  • PTEN Hamartoma Tumor Syndrome (protocolSection.conditionsModule.conditions)
  • Retinoblastoma (protocolSection.conditionsModule.conditions)
  • Rhabdoid Tumor Predisposition Syndrome (protocolSection.conditionsModule.conditions)
  • Rhabdomyosarcoma (protocolSection.conditionsModule.conditions)
  • Rothmund-Thomson Syndrome (protocolSection.conditionsModule.conditions)
  • Tuberous Sclerosis (protocolSection.conditionsModule.conditions)
  • Von Hippel-Lindau Disease (protocolSection.conditionsModule.conditions)

Intervention details are not present in the imported fields for this record. No drug-condition relationship is inferred from co-listing.

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