Identification, Molecular Epidemiology Angiosarcoma of the Liver France

NCT01786889 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 9

Last updated 2016-07-29

No results posted yet for this study

Summary

The purpose of this study is to test the feasibility of identifying incident cases of angiosarcoma of the liver from the network NetSarc.

Conditions

  • Angiosarcoma

Interventions

BIOLOGICAL

blood and urine

Blood collection and urine collection after consent of the patient

BEHAVIORAL

Questionnaire

The patient complete the questionnaire alone at home

BEHAVIORAL

Telephone interview

The patient will be contacted by the CRA for a telephone interview of around one hour

Sponsors & Collaborators

  • Institut de Veille Sanitaire

    collaborator UNKNOWN
  • Centre Oscar Lambret

    lead OTHER

Principal Investigators

  • LE MOAL Joelle, Dr · Institut de Veille Sanitaire_Département Santé Environnement

  • PENEL Nicolas, MD · Centre Oscar Lambret

Study Design

Allocation
NA
Purpose
PREVENTION
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-06-30
Primary Completion
2016-09-30
Completion
2017-01-31

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01786889 on ClinicalTrials.gov