The scope of the trial is to predict the early complete clinical response to exclusive
concomitant radiochemotherapy in esophageal cancer by the study of the pre- and per-
therapeutic proteomic profile.
Procedure: Blood sampling
Drug: Chemotherapy (Fluorouracil and Cisplatin)
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Locations near you
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Full eligibility criteria for NCT00911092
Ages eligible for Study
18 Years and older
Genders eligible for Study
Accepts Healthy Volunteers
Invasive esophageal carcinoma at any stage (all T, N0 or N1, M0 or M1a), histologically proven
Treated by exclusive concomitant radiochemotherapy
Inclusion in a clinical trial with an experimental drug during the study and until 15 weeks after the end of radiotherapy)
All locations for NCT00911092
Centre Paul Papin
Angers, France, 49933
Centre Hospitalier Universitaire
Brest, France, 29200
Centre François BACLESSE
Caen, France, 14046
Centre Oscar Lambret
Lille, France, 59020
Centre Eugène Marquis
Rennes, France, 35042
CHU - Hopital Charles Nicolle
Rouen, France, 76031
View full eligibility
Tris trial is registered with FDA with number: NCT00911092. The sponsor of the trial is Centre Oscar Lambret and it is looking for 50 volunteers for the current phase.
Official trial title: Study of Predictive Proteomic Factors of the Response to Exclusive Concomitant Radiochemotherapy in Oesophageal Cancer
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