Recipient Site Pre-conditioning in Fat Grafting (NCT03393598) | Clinical Trial Compass
CompletedNot Applicable
Recipient Site Pre-conditioning in Fat Grafting
Switzerland60 participantsStarted 2018-01-08
Plain-language summary
This study aims to investigate the preparation of the recipient site prior to autologous fat grafting (AFG) using different methods.
Who can participate
Age range18 Years – 65 Years
SexFEMALE
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Inclusion Criteria:
* 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 Criteria:
* 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.