Preoperative Radiation Therapy and Immediate Breast Reconstruction
Recruiting
N/A
Interventional Study
Breast Neoplasms
Breast Carcinoma
Breast Adenocarcinoma
Cancer
Neoplasm
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Female
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 180 (estimated)
- Sponsor
- Cancer Research Antwerp · Other
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About This Trial
The goal of this phase III randomized controlled trial (PRADAIIBE) is to assess if preoperative radiation therapy (Preop-RT) combined with immediate breast reconstruction (IBR) can safely improve both aesthetic and quality of life outcomes in breast cancer patients, compared to the standard of care (SoC) therapy consisting of post-mastectomy radiation therapy (PMRT) and delayed/immediate breast re…
Trial Locations
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Eligibility Criteria
Screening assessments, including review of all study eligibility criteria must be completed before enrolment and randomisation.
Inclusion criteria:
In order to be eligible to participate in this study, a participant must meet all of the following criteria:
1\. Women ≥18 years with histopathologic…
Contacts