Status:
COMPLETED
Recipient Site Pre-conditioning in Fat Grafting
Lead Sponsor:
University Hospital, Basel, Switzerland
Collaborating Sponsors:
Clinical Trial Unit, University Hospital Basel, Switzerland
Ospedale Regionale di Lugano
Conditions:
Graft Loss
Condition
Eligibility:
FEMALE
18-65 years
Phase:
NA
Brief Summary
This study aims to investigate the preparation of the recipient site prior to autologous fat grafting (AFG) using different methods.
Detailed Description
Autologous fat grafting is emerging as a powerful tool for soft tissue reconstruction and augmentation and is widely used in plastic surgery. However, there is great variability in terms of long-term ...
Eligibility Criteria
Inclusion
- Informed Consent as documented by signature
- Patients presenting with contracted scars or body contouring deformities, especially as a result of previous radiation therapy or infection, in and around the breast.
- Body mass index superior than 18.5
Exclusion
- Need for antiplatelets drugs in the 5 days before surgery and 3 days after,
- Known or suspected non-compliance, drug or alcohol abuse,
- Inability to follow the procedures of the study due to language problems, psychological disorders, dementia of the participant,
- Previous enrolment into the current study,
- Enrolment of the investigator, his or her family members, employees and other dependent persons,
- Patients with haemorrhagic diatheses.
Key Trial Info
Start Date :
January 8 2018
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
April 11 2024
Estimated Enrollment :
60 Patients enrolled
Trial Details
Trial ID
NCT03393598
Start Date
January 8 2018
End Date
April 11 2024
Last Update
March 12 2025
Active Locations (2)
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1
University Hospital Switzerland, Dept. of plastic, reconstructive, aestetic and hand surgery
Basel, Switzerland, 4031
2
Klinik Hirslanden, Plastic Surgery Group AG
Zurich, Switzerland