International Prospective REgistry on Pre-pectorAl Breast REconstruction
Recruiting now
Conditions studied: Breast Cancer
In brief
This is an international multicenter prospective cohort study aimed at collecting data on breast reconstruction techniques with pre-pectoral implants after mastectomy for breast cancer. The aim of the study is to collect data on the surgical, aesthetic and oncological results, as well as on the quality of life of the patients who will undergo breast reconstruction with a pre-pectoral approach.
Key facts
- Study ID
- NCT05817175
- Run by
- IRCCS San Raffaele
- People needed
- 1236
- Starts
- 2023-09-12
- Expected to finish
- 2027-09-10
- Last updated by the study team
- 2025-06-04
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Female patients older than 18 years old
- Signed informed consent form
- Patients undergoing mono or bilateral therapeutic mastectomy
- Patients undergoing pre-pectoral implant-based breast reconstruction with implant or expander with or without mesh
You may not qualify if…
- Male patients
- Patients not suitable for surgical treatment
- Patients undergoing subpectoral reconstruction
- Patients undergoing breast reconstruction with autologous tissue.
Where it is running
- Univesidad de Buenos Aires — Buenos Aires, Argentina (enrolling)
- Mansoura Insurance — Al Mansurah, Egypt (enrolling)
- Mansoura Oncology — Al Mansurah, Egypt (enrolling)
- National ans Kapodistrian University of Athens — Athens, Greece (enrolling)
- Ospedale San Raffaele — Milan, MI, Italy (enrolling)
- Fondazione Policlinico Universitario Agostino Gemelli — Roma, RM, Italy (enrolling)
- University Hospital of Karol Marcinkowski — Zielona Góra, Poland (enrolling)
- Prof. Dr. Ion Chiricuta Institute of Oncology — Cluj-Napoca, Romania (enrolling)
- Hospital del Mar — Barcelona, Spain (enrolling)
- Marmara University School of medicine — Istanbul, Turkey (Türkiye) (enrolling)
- University Hospitals of Leicester — Leicester, United Kingdom (enrolling)
Full record on ClinicalTrials.gov
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