Phase
Condition
Breast Reconstruction
Treatment
Treatment with Omnistrip®
Treatment with NovoX® Cup
Clinical Study ID
Ages > 18 Female
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Written informed consent
Female patients 18 years and older
Patient able to give informed consent
Patients undergoing bilateral breast reduction
Exclusion
Exclusion Criteria:
Absent informed consent
Patients from protected groups and those who are not personally able to giveconsent.
Patients younger than 18 years
Pregnancy (pregnancy test before enrollment) and breastfeeding women
Former radiation of the breast(s)
Former surgery at the operation site
Skin abnormalities in the operation area (e.g. burn scars)
Participation in other clinical trials during this study
Active malignant disease
Breast cancer history
Radiation or chemotherapy during the study period or up to 6 months before possibleenrollment
Immune disease
Study Design
Study Description
Connect with a study center
Division of Plastic, Aesthetic & Reconstructive Surgery, Department of Surgery, Medical University of Graz
Graz, A-8036
AustriaActive - Recruiting
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