EUBREAST 11 (R) I-PREPARE (International Prospective REgistry on Pre-PectorAL REconstruction)

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EUBREAST 11 (R) I-PREPARE Trial Design: International prospective cohort study that aims at comparatively evaluating data on different surgical techniques of pre-pectoral breast reconstruction with or without radiation Primary Endpoint: Implant-loss at three months postoperatively defined as the unplanned removal or loss of the implant as a result of infection or other complication
Below please find

Project registration number

https://ichgcp.net/clinical-trials-registry/NCT05817175

Project Description

  • Study PI: Oreste Gentilini
  • Study initiated by EUBREAST
  • Trial Design:  International prospective cohort study that aims at comparatively evaluating data on different surgical techniques of
    pre-pectoral breast reconstruction with or without radiation
  • Primary Endpoint:  Implant-loss at three months postoperatively defined as the unplanned removal
    or loss of the implant as a result of infection or other complication

For more information regarding this study, please contact goldman@eubreast.com

The International Steering Board

Principal Investigator

Dr Oreste Gentilini – San Raffaele University and Research Hospital, Milan, Italy

Supporting Organizations

ANISC – AWO-Gyn – ESTRO – EUROPA DONNA – GRETA – iBRA-NET – IPOS – OPBC – SENATURK

Documents for Downloads (in English)

I-PREPARE STUDY PROTOCOL – AMENDMENT V. 3

I-PREPARE ABSTRACT

Studio Initiation Video

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