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Phase II Prospective, Open Label Randomized Controlled Trial Comparing Standard of Care Therapy With and Without Sequential Cytoreductive Intervention for Patients With Metastatic Foregut Adenocarcinoma and Undetectable Circulating Tumor-Deoxyribose Nucleic Acid (ctDNA) Levels

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT07282912
Title field or adapter rule
{'original_value': 'Phase II Prospective, Open Label Randomized Controlled Trial Comparing Standard of Care Therapy With and Without Sequential Cytoreductive Intervention for Patients With Metastatic Foregut Adenocarcinoma and Undetectable Circulating Tumor-Deoxyribose Nucleic Acid (ctDNA) Levels', 'source_field': 'protocolSection.identificationModule.officialTitle'}
Ingested At
2026-10-31T23:27:26.447335+00:00
Published At
2026-09-08T00:00:00+00:00
Record Updated At
2026-09-08
Source Retrieved At
2026-10-31T22:17:58.991924+00:00
Timestamp Basis
ClinicalTrials.gov API/RSS response retrieval timestamp recorded by Dossier adapter
Date limitation
ClinicalTrials.gov API/RSS response retrieval timestamp recorded by Dossier adapter

Fields recorded by this source

protocolSection.conditionsModule.conditions
["Foregut Adenocarcinoma", "Esophageal Adenocarcinoma", "Gastroesophageal Adenocarcinoma", "Gastric Adenocarcinoma", "Pancreas Adenocarcinoma", "Duodenal Adenocarcinoma", "Ampullary Adenocarcinoma", "Gallbladder Adenocarcinoma", "Intra - and Extrahepatic Cholangiocarcinoma"]
protocolSection.statusModule.lastUpdatePostDateStruct
{"date": "2026-09-08", "type": "ACTUAL"}
protocolSection.identificationModule.nctId
"NCT07282912"
protocolSection.identificationModule.officialTitle
"Phase II Prospective, Open Label Randomized Controlled Trial Comparing Standard of Care Therapy With and Without Sequential Cytoreductive Intervention for Patients With Metastatic Foregut Adenocarcinoma and Undetectable Circulating Tumor-Deoxyribose Nucleic Acid (ctDNA) Levels"
protocolSection.statusModule.overallStatus
"RECRUITING"
protocolSection.designModule.phases
["PHASE2"]
protocolSection.statusModule.resultsFirstPostDateStruct
null

Study condition terms

  • Foregut Adenocarcinoma (protocolSection.conditionsModule.conditions)
  • Esophageal Adenocarcinoma (protocolSection.conditionsModule.conditions)
  • Gastroesophageal Adenocarcinoma (protocolSection.conditionsModule.conditions)
  • Gastric Adenocarcinoma (protocolSection.conditionsModule.conditions)
  • Pancreas Adenocarcinoma (protocolSection.conditionsModule.conditions)
  • Duodenal Adenocarcinoma (protocolSection.conditionsModule.conditions)
  • Ampullary Adenocarcinoma (protocolSection.conditionsModule.conditions)
  • Gallbladder Adenocarcinoma (protocolSection.conditionsModule.conditions)
  • Intra - and Extrahepatic Cholangiocarcinoma (protocolSection.conditionsModule.conditions)

Interventions recorded in this study

  • {'armGroupLabels': ['Sequential cytoreductive intervention'], 'description': 'A treatment plan that involves multiple procedures given one after another to remove cancerous tumors depending on metastasis.', 'name': 'Sequential cytoreductive intervention', 'type': 'PROCEDURE'} (protocolSection.armsInterventionsModule.interventions[])
  • {'armGroupLabels': ['Sequential cytoreductive intervention', 'Standard of care'], 'description': 'A personalized blood test that detects circulating tumor DNA (ctDNA) to monitor for molecular residual disease (MRD) in patients who have been diagnosed with cancer.', 'name': 'Signatera Genome ultra-sensitive ctDNA blood test', 'type': 'DIAGNOSTIC_TEST'} (protocolSection.armsInterventionsModule.interventions[])

An intervention appearing in a study record does not establish an effect or an approved use.

This index keeps the source fields it imported; it may not contain the complete original record. Verify wording and context in the linked source.