ClinicalTrials.Veeva

Menu

Platelet Rich Fibrin Versus Platelet Rich Plasma for Microneedling Treatment of Facial Photoaging

Chang Gung Medical Foundation logo

Chang Gung Medical Foundation

Status

Not yet enrolling

Conditions

Photoaging

Treatments

Procedure: platelet-rich palsma
Procedure: platelet-rich fibin

Study type

Interventional

Funder types

Other

Identifiers

NCT06452667
CPRPG5P0011

Details and patient eligibility

About

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.

Enrollment

30 estimated patients

Sex

All

Ages

20+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Men or female patients older than 20 years old with facial photoaging (Glogau Scale type II)
  2. The photoaging severity of bilateral face is symmetric.

Exclusion criteria

  1. Patients with thrombocytopenia, coagulopathy, hematopoietic malignancy.
  2. Patients with severe inflammation over treated area, malignancy, keloid, or poor wound healing history.
  3. Patients had received laser, radiofrequency, ultherapy over treated area within 6 months.
  4. Patients had received botulism or filler injection over treated area within 12 months.
  5. Patients had received plastic surgery over treated area within 12 months.
  6. Patients had severe psychiatric disorders with poor control.
  7. Patients with other diseases which are not suitable for receiving platelet rich plasma (PRP) or platelet rich fibrin (PRF) therapy.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

30 participants in 2 patient groups

platelet-rich fibin
Experimental group
Description:
Each case will receive 3 sessions of therapies with one month interval. We will apply 1-2ml PRF to the photoaging areas in one side of the cheek of patients by using microneedling.
Treatment:
Procedure: platelet-rich fibin
platelet-rich palsma
Active Comparator group
Description:
Each case will receive 3 sessions of therapies with one month interval. We will apply 1-2ml PRP to the photoaging areas in one side of the cheek of patients by using microneedling.
Treatment:
Procedure: platelet-rich palsma

Trial contacts and locations

1

Loading...

Central trial contact

Yau-Li Huang, MD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2025 Veeva Systems