Split Face Study of the Effects of Micro Needling With and Without Platelet Rich Plasma
Stopped early · Not applicable
Conditions studied: Aging
In brief
This pilot study will expand knowledge and application of 2 X concentration of Platelet Rich Plasma (PRP) in conjunction with microneedling using the SkinPen device.
Key facts
- Study ID
- NCT04219293
- Run by
- Dallas Plastic Surgery Institute
- People needed
- 23
- Starts
- 2019-08-26
- Expected to finish
- 2020-02-01
- Last updated by the study team
- 2021-08-11
Who can join
Age: 30 and older, up to 60. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Healthy males and females ages 30-60 years old.
- No previous minimally invasive or invasive skin resurfacing within the prior 12 months (i.e. fractionated laser, ablated laser, chemical peels, microneedling, etc…
- VisiaTM Scan showing aging including skin texture, wrinkles, brown spots, and pores.
- Patient willing to sign informed consent.
You may not qualify if…
- Keloid scars;
- History of eczema in treatment area; psoriasis and any other chronic skin conditions the Investigator determines disqualifies the patient for participation in treatment area;
- History of actinic (solar) keratosis in treatment area;
- History of hemophilia;
- History of diabetes;
- The presence of raised moles, warts on the targeted area.
- Absolute contraindications include; scleroderma, collagen vascular diseases or cardiac abnormalities; blood clotting problems; active bacterial or fungal infection; facial melanosis; malignant tumors, immunosuppression; use of blood thinners or prednisone; pregnant or nursing women; corticosteroids within two weeks of the procedure, chronic liver disease, porphyria or other skin diseases.
- Patient not willing to sign informed consent.
Where it is running
- Dallas Plastic Surgery Institute — Dallas, Texas, United States
Full record on ClinicalTrials.gov
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