About this trial
The present study was conducted for analyzing the efficacy and safety of platelet-rich plasma (PRP) and platelet-rich fibrin (PRF) in photoaging therapy.
Specific arms:
1. The investigators will compare the photoaging improvement of PRF and PRP treated face before and after treatment by two blinded investigators. 2. The investigators will evaluate the improvement of each parameter of photoaging by Visia system, dermoscope, and optical coherence tomography. 3. The investigators will evaluate the safety of the treatment of PRF and PRP.
Each case will receive 3 sessions of injection therapies with one month interval (T0, T1, and T2). Each case will receive PRP therapy on one side of the face and PRF on the other side of face. The investigators will determine the treatment method for both sides of each case randomly by coin flapping before the study. The investigators will evaluate each case before each session of therapy (T0, T1, T2) as well as 1 (T3) and 3 months (T4) after final session of treatment.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Men or female patients older than 20 years old with facial photoaging (Glogau Scale type II)
The photoaging severity of bilateral face is symmetric.
Disqualifiers
Patients with thrombocytopenia, coagulopathy, hematopoietic malignancy.
Patients with severe inflammation over treated area, malignancy, keloid, or poor wound healing history.
Patients had received laser, radiofrequency, ultherapy over treated area within 6 months.
Patients had received botulism or filler injection over treated area within 12 months.
Trial design
Parallel
Treatments tested in this trial
platelet-rich fibin
Procedure/SurgeryEach case will receive 3 sessions of microneedling therapies with one month interval. Each case will receive platelet-rich fibin therapy on one side of the face. The other side of the face was treated with platelet-rich palsma.
platelet-rich palsma
Procedure/SurgeryEach case will receive 3 sessions of microneedling therapies with one month interval. Each case will receive platelet-rich palsma therapy on one side of the face. The other side of the face was treated with platelet-rich fibin.
Treatment groups
Trial outcomes
Primary outcomes
Global Aesthetic Improvement Scale
We will compare the photoaging improvement of PRF and PRP treated face before treatment and 3 months after last treatment by two blinded investigators using Global Aesthetic Improvement Scale (GAIS). GAIS, which is a 5-point scale wherein 5 = very much improved, 4 = much improved, 3 = improved, 2 = no change, and 1= worse.
Secondary outcomes
Fitzpatrick wrinkle scale
To assess the severity of wrinkles of photoaging areas (minimum: 1, mild; maximum: 9, severe)
Wrinkle Severity Rating scale
To assess the severity of wrinkles of photoaging areas (minimum: 1, absent; maximum: 5, extreme)
Other outcomes
The scores of rhytids in VISIA system
Apply the scores of different aging domains in VISIA system for evaluating the therapeutic response. (minimum: 1, worse; maximum: 100, severe)
The scores of Textures in VISIA system
Apply the scores of different aging domains in VISIA system for evaluating the therapeutic response. (minimum: 1, worse; maximum: 100, severe)
The scores of Pores size in VISIA system
Apply the scores of different aging domains in VISIA system for evaluating the therapeutic response. (minimum: 1, worse; maximum: 100, severe)
The scores of Brown spots in VISIA system
Apply the scores of different aging domains in VISIA system for evaluating the therapeutic response. (minimum: 1, worse; maximum: 100, severe)
Sponsors and contacts
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