Randomized, Multicenter, Phase III Trial to Assess Conformal Post-operative Radiotherapy vs. Surveillance After Complete Resection of Stage II/III Thymoma (RADIO-RYTHMIC-01)

Abroad (travel likely)Recruiting

Conditions

Thymoma Malignant Recurrent

Simple summaryAI-assisted

This summary is produced by a language model and is experimental. It may be incomplete or inaccurate and is not a substitute for professional medical advice.

Locations
  • CHU Caen, Caen, France

    Contact: Study coordinator (Simon DESHAYES, MD)
    Contact: Principal Investigator (Simon DESHAYES, MD)
  • CLCC François BACLESSE, Caen, France

    Contact: Study coordinator (Delphine LEROUGE, MD)
    Contact: Principal Investigator (Delphine LEROUGE, MD)
  • CLCC Georges François Leclerc, Dijon, France

    Contact: Study coordinator (Etienne MARTIN, MD)
    Contact: Principal Investigator (Etienne MARTIN, MD)
  • Centre Oscar Lambret, Lille, France

    Contact: Study coordinator (Florence LE TINIER, MD)
    Contact: Principal Investigator (Florence LE TINIER, MD)
  • CHU Lyon, Lyon, France

    Contact: Study coordinator (Thomas PIERRET, MD)
    Contact: Principal Investigator (Thomas PIERRET, MD)
  • AP-HM Hôpital Nord, Marseille, France

    Contact: Study coordinator (Pascal THOMAS, Pr)
    Contact: Principal Investigator (Pascal THOMAS, Pr)
  • Institut du Cancer de Montpellier, Montpellier, France

    Contact: Study coordinator (Xavier QUANTIN, Pr)
    Contact: Principal Investigator (Xavier QUANTIN, Pr)
  • Antoine LACASSAGNE, Nice, France

    Contact: Study coordinator (Jérôme DOYEN, MD)
    Contact: Principal Investigator (Jérôme DOYEN, MD)
  • Institut Curie, Paris, France

    Contact: Study coordinator (Nicolas GIRARD, PR) · nicolas.girard2@curie.fr
    Contact: Principal Investigator (Nicolas GIRARD, PR)
  • Hôpital Européen Georges Pompidou, Paris, France

    Contact: Study coordinator (Aurélia ALATI, MD)
    Contact: Principal Investigator (Aurélia ALATI, MD)
  • Hôpital Bichat AP-HP, Paris, France

    Contact: Study coordinator (Valérie GOUNANT, Pr)
    Contact: Principal Investigator (Valérie GOUNANT, Pr)
  • CHU Haut Lévêque, Pessac, France

    Contact: Study coordinator (POUYPOUDAT, MD)
    Contact: Principal Investigator (Claudia POUYPOUDAT, MD)
  • CHU Rennes Hôpital Sud, Rennes, France

    Contact: Study coordinator (Charles RICORDEL, MD)
    Contact: Principal Investigator (Charles RICORDEL, MD)
  • CHU Rouen, Rouen, France

  • CLCC Henri Becquerel, Rouen, France

    Contact: Study coordinator (Sébastien THUREAU, MD)
    Contact: Principal Investigator (Sébastien THUREAU, MD)
  • Institut de Cancérologie de l'Ouest, Saint-Herblain, France

    Contact: Study coordinator (François THILLAYS, MD)
    Contact: Principal Investigator (François THILLAYS, Pr)
  • CHU Strasbourg, Strasbourg, France

    Contact: Study coordinator (Pierre-Emmanuel FALCOZ, Pr)
    Contact: Principal Investigator (Pierre-Emmanuel FALCOZ, Pr)
  • Institut Claudius Regaud, Toulouse, France

    Contact: Study coordinator (Jonathan KHALIFA, MD)
    Contact: Principal Investigator (Jonathan KHALIFA, MD)
  • CHRU Tours, Tours, France

    Contact: Study coordinator (Eric PICHON, MD)
    Contact: Principal Investigator (Eric PICHON, MD)
  • Institut de Cancérologie de Lorraine Nancy, Vandœuvre-lès-Nancy, France

    Contact: Study coordinator (Mathilde CUENIN, MD)
    Contact: Principal Investigator (Mathilde CUENIN, MD)
  • Gustave Roussy, Villejuif, France

    Contact: Study coordinator (Angela BOTTICELLA, MD)
    Contact: Principal Investigator (Angela BOTTICELLA, MD)