Cancer, Breast Clinical Trial
Official title:
The Role of Lipofilling After Oncoplastic Breast Surgeries : Evaluation of Outcomes and Patient Satisfaction
Verified date | June 2022 |
Source | Assiut University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The Role of Lipofilling After Oncoplastic Breast surgeries : Evaluation of Outcomes and Patient Satisfaction
Status | Recruiting |
Enrollment | 20 |
Est. completion date | September 1, 2024 |
Est. primary completion date | March 1, 2024 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years to 50 Years |
Eligibility | Inclusion Criteria: Female gender. Age of 18 years and older. History or in candidate for a mastectomy in the near future. Patients undergoing prophylactic mastectomy. Patients' choice to undergo a breast reconstruction. Wanting to participate in this study. Patient is able to wear the BRAVA (BRA like VAcuum-based external tissue expander) device. Exclusion Criteria: Active smoker or a history of smoking 4 weeks prior to surgery. Current substance abuse. History of lidocaine allergy. Four weeks or less after chemotherapy. History of radiation therapy in the breast region. Oncological treatment includes radiotherapy after mastectomy. Kidney disease. Steroid dependent (daily or weekly). Immune-suppressed or immune-compromised disease. Uncontrolled diabetes. body mass index of >30. Large breast size (ie, larger than cup C), unless the patient prefers reduction of the contralateral side towards cup C. Extracapsular silicone leaking from the encapsulated implant from a previous breast reconstruction. |
Country | Name | City | State |
---|---|---|---|
Egypt | Assiut university | Assiut |
Lead Sponsor | Collaborator |
---|---|
Assiut University |
Egypt,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Cosmetic apperance | Volumetric evaluation of breast after surgery and symmetry to the other breast | 1 week | |
Secondary | Complications during the treatment and follow up | Complications during the treatment Follow-up period will be registered and compared between the intervention and control groups | 1 month |
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