None listed
Conditions
Brief summary
Fat grafting is the procedure of choice for contour deformity. There are different studies showing different results about fat survival. This study will be aimed to find the autologous fat survival when used with or without PRP. The second outcome parameter of scar remodeling effect of the fat will be observed in this study.
Interventions
In group A, Fat Graft with PRP will be used. The fat will be harvested by consultant Plastic Surgeon from medial thigh. The procedure will done under local anesthesia. The duration of procedure will be around 60 minutes. The procedure will be done to correct the contour deformity of the patients by filling the fat in different layers of skin and underlying tissue in single procedure. Tumescent or infiltration Solution was made of 0.5% lidocaine with 1:200000 epinephrine diluted in 200 ml lactate ringer solution. This was injected with 17 G cannula in subcutaneous tissue of donor area. The injection and harvesting was done at 2:1. The fat with 23G cannula was harvested and prepared with the help of gravity. The fat separated from fluid and oil. The PRP will be obtained from the blood of the patient, 20 ml of blood will be obtained by the technician at the start of the procedure before harvesting the fat. The blood will be centrifuge at 1500 revolutions for 5 minutes and then at 2500 revolutions for 10 minutes. The plasma will be separated. 5 cc of adipocytes + 3 ml of PRP in 10 ml syringes with adding 10% CaCl (0.05 cm3 of CaCl per 3 ml). The extracted fat will be injected with 1cc syringe attached to 14 G needle in multiple layers. 20-30% over correction of contour deformity was done because of chance of absorption. At the end of the procedure, the steri strip over the recipient and dressing for donor sites was applied.
Sponsors
Study design
Eligibility
Inclusion criteria
At least 2 separate (i.e. non-contiguous) or 1 large wound/scar previously healed by placement of a STSG and/or by secondary intention ("study sites"), each Less than or equal to 80 cm2 in size (area).The sites should be similar in size and anatomical location (e.g. upper arms; trunk; legs) to the extent practically possible. Adequate adipose available for harvesting
Exclusion criteria
1. Life or limb-threatening injury/disease determined on history and clinical examination. 2. Active drug use/abuse determined on history 3. Pregnancy confirmed on urine test. 4. History of bleeding tendency/inability to clot,determined on PT, APTT and/or INR more than or equal to 2.2. 5. Smoking will be assessed on history