Hypertrophic Scar Clinical Trial
Official title:
Nanofat on Wound Healing and Scar Formation: a Randomized, Split-scar, Double Blind Trial
This study will evaluate the effectiveness and safety of intradermal injection of Nanofat on wound healing and scar formation.
In this monocentric, randomized, controlled, double-blinded prospective interventional study,
twenty patients will be included. Each patient will be his/her own control.
Patients undergoing DIEPflap breast reconstruction will be included in this study. During the
surgery, the abdominal incision will be divided in two equal sides with the umbilicus as
midline reference. The sides will be randomized in a treatment side and control side. The
treatment side will receive intradermal nanofat injections after the subcutaneous and right
before the intradermal sutures.
The patient and investigators will be blinded for the treatment protocol. The effects on
wound healing, adverse events, scar formation and pigmentation will be evaluated up to one
year after the surgery.
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