The French EsoGastricTumours Data Base

  • STATUS
    Recruiting
  • End date
    May 17, 2027
  • participants needed
    15000
  • sponsor
    University Hospital, Lille
Updated on 17 September 2020
Investigator
Guillaume PIESSEN, MD; PHD
Primary Contact
Centre Hospitalier Universitaire (0.0 mi away) Contact
+36 other location
cancer
esophageal cancer

Summary

This retrospective study aims at evaluating the outcomes of gastrointestinal stromal tumor after surgery.

Details
Clinical Study IdentifierNCT02526095
SponsorUniversity Hospital, Lille
Last Modified on17 September 2020

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Eligibility

Yes No Not Sure

Inclusion Criteria

Is your age between 18 yrs and 90 yrs?
Gender: Male or Female
Do you have any of these conditions: Esophageal Diseases or Esophageal Disorders?
Patient with
esophageal cancer, gastric or gastroesophageal junction diagnosed biopsy , regardless of the subtype of cancer, tumor stage or treatment envisaged
Naive treatment for this cancer
Naive treatment for this cancer , failing that received neoadjuvant treatment
Male or female 18 years
social protection scheme
sign a free and informed consent for blood sampling , the different questionnaires and the collection of patient information

Exclusion Criteria

Male or female aged ( e) under 18 years
Private person of liberty or under supervision (including guardianship )
People who do not speak French
Major Nobody unable to consent
Patient FREGAT already included in the base
Patient Refusal
Clear my responses

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Step 2 Get screened

Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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Step 3 Enroll in the clinical study

If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Step 4 Get your study results

Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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