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NCT03957031Completed

Gastric Cancer Risk Factors Associated With EU and CELAC Populations

Source: ClinicalTrials.gov · Last updated 9 May 2024

Brief summary (registry, in English)

The study uses a case-control design that examines the differences in types of exposures between cases defined with a pathological confirmation of GC diagnosis, and controls, defined as patients to whom a gastroscopy was indicated and confirmed absent of GC i

Status (registry)
Completed
Study type
Observational
Enrollment
1600 (actual)
First submitted
17 May 2019
Start date
31 May 2019
Primary completion date
31 Dec 2023
Lead sponsor
Fundación para la Investigación del Hospital Clínico de Valencia
NCT number
NCT03957031

What you commit to

  • Study type: Observational
  • Participants enrolled: 1600
  • From 31 May 2019 to the primary completion date, 31 Dec 2023
  • 8 sites in 7 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study design.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Criteria the registry did not label

  • Cases
  • Inclusion criteria
    • Subjects ≥18 years old.
    • GC diagnosis (including gastroesophageal junction cancer) from IPATIMUP, INCAN, VUMC, PUC, VHIO, IAF, INCLIVA and GENPAT centres, in the last six months before his/her inclusion in the study.
    • Has given and signed the IC to participate in this study.
  • Exclusion criteria:
    • Patients diagnosed with GC (including gastroesophageal junction cancer) from other centres/ countries not participating in this proposal.
    • Patients with suspected with GC diagnosis but not confirmed by the pathological report.
    • Controls
  • Inclusion criteria
    • Subjects ≥18 years old.
    • Subjects to whom a gastroscopy was indicated in its medical care and confirmed absent of GC in the same centres will be matched in age (+/- 10 years), gender and pertaining from the same region of the GC case. Thus, to match our GC cases same number of controls is expected to be recruited.
    • Has given and signed the IC to participate in this study.
  • Exclusion criteria:
    • Subjects from a different geographic area from the cases.
    • Patients with high suspicion of GC (including gastroesophageal junction cancer) or previous personal history known of document chronic gastritis diagnosed by endoscopy and confirmed by histology.

Age in the registry: 18 years to 90 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (8)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Instituto Alexander Fleming
Coordinator of this site? Confirm its status
Buenos AiresArgentinaUnknown status
Pontificia Universidad Catolica de Chile
Coordinator of this site? Confirm its status
SantiagoChileUnknown status
Fundació Privada Institut d'Investigació Oncològica de Vall-Hebron (VHIO)
Coordinator of this site? Confirm its status
BarcelonaSpainUnknown status
Hospital Clinico Universitario de Valencia
Coordinator of this site? Confirm its status
ValenciaSpainUnknown status
Instituto Nacional de Cancerologia
Coordinator of this site? Confirm its status
Mexico CityMexicoUnknown status
VU Medical Centre
Coordinator of this site? Confirm its status
AmsterdamNetherlandsUnknown status
Institute of Pathology and Immunology of University of Porto
Coordinator of this site? Confirm its status
PortoPortugalUnknown status
GenPat
Coordinator of this site? Confirm its status
AsunciónParaguayUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.