Platelet Rich Plasma for Treatment of Facial Photoaging: A Double-blind, Randomized, Split-face Study

October 24, 2021 updated by: Chang Gung Memorial Hospital

Chang Gung Memorial Hospital, Taipei, Taiwan

Photoaging is characterized by cellular changes and alterations in dermal extracellular matrix proteins with degeneration of connective tissue caused by intrinsic and extrinsic factors. The clinical manifestations of photoaging included wrinkles, pigmented changes, tissue loss, and sagging. Autologous platelet-rich plasma is a preparation of platelets in concentrated plasma from peripheral blood. The α granules of platelets contained many growth factors. According to previous literature, growth factors in platelet-rich plasma directly stimulate fibroblast proliferation to boost collagen production. It has also been shown to modulate extracellular matrix metabolism and remodeling by increasing the expression of specific matrix metalloproteinases. In review of previous literatures, there was only limited researches of platelet-rich plasma for treatment of photoaging. Therefore, the present study was conducted for analyzing the efficacy and safety of autologous platelet-rich plasma in photoaging therapy.

Study Overview

Detailed Description

Autologous platelet-rich plasma is a preparation of platelets in concentrated plasma from peripheral blood. The α granules of platelets contained many growth factors, such as platelet-derived growth factor, transforming growth factor, vascular endothelial growth factor, and epithelial growth factor. These growth factors can trigger intracellular signaling cascades that ultimately alter gene expression and protein synthesis. Clinically, autologous platelet-rich plasma has been applied for treatment of hair loss, chronic wounds, and atrophic scars.

Photoaging is characterized by cellular changes and alterations in dermal extracellular matrix proteins with degeneration of connective tissue caused by intrinsic and extrinsic factors. The clinical manifestations of photoaging included wrinkles, pigmented changes, tissue loss, and sagging. The therapeutic modalities of photoaging included energy-based device, filler injection, and surgical treatment. However, there are some limitations and drawbacks of these therapies. For example, filler injection may cause foreign body granuloma, vascular occlusions, or tissue necrosis. Surgical treatment is an invasive procedure which may cause hematoma, infection, or scar formation.

According to previous literature, growth factors in platelet-rich plasma directly stimulate fibroblast proliferation to boost collagen production. It has also been shown to modulate extracellular matrix metabolism and remodeling by increasing the expression of specific matrix metalloproteinases. Platelet-rich plasma-enhanced expression of matrix metalloproteinases -1 and -3 helps clear photodamaged extracellular matrix components and allow for a better quality, more organized collagen meshwork. This process helps soften fine lines and minimize scarring. In addition, transforming growth factor and epithelial growth factor in platelet-rich plasma are known to modulate keratinocyte propagation and migration as well as repair barrier function. In review of previous literatures, there was only limited researches of platelet-rich plasma for treatment of photoaging. Therefore, the present study was conducted for analyzing the efficacy and safety of autologous platelet-rich plasma in photoaging therapy.

Study Type

Interventional

Enrollment (Anticipated)

15

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

16 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

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) injection therapy.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Triple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: platelet rich plasma
Each case will receive 3 sessions of injection therapies with one month interval. The practitioner will inject 2ml of platelet rich plasma with fan and linear method into photoaging areas in one side of the midface in one session of treatment.
Each case will receive 3 sessions of injection therapies with one month interval. Each case will receive platelet rich plasma therapy on one side of the face. The other side of the face was treated with platelet poor plasma.
Other: platelet poor plasma
Each case will receive 3 sessions of injection therapies with one month interval. The practitioner will inject 2ml of platelet rich plasma with fan and linear method into photoaging areas in the other side of the midface in one session of treatment.
Each case will receive 3 sessions of injection therapies with one month interval. Each case will receive platelet rich plasma therapy on one side of the face. The other side of the face was treated with platelet poor plasma.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Global Aesthetic Improvement Scale
Time Frame: 3 months after the last session of treatment
To assess the global aesthetic improvement in appearance compared to pretreatment (minimum: -1, worse; maximum: 3, very much improved)
3 months after the last session of treatment
Fitzpatrick wrinkle scale
Time Frame: 3 months after the last session of treatment
To assess the severity of wrinkles of photoaging areas (minimum: 1, mild; maximum: 9, severe)
3 months after the last session of treatment
Wrinkle Severity Rating scale
Time Frame: 3 months after the last session of treatment
To assess the severity of wrinkles of photoaging areas (minimum: 1, absent; maximum: 5, extreme)
3 months after the last session of treatment

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The scores of rhytids in VISIA system
Time Frame: before the 1st, 2nd and 3rd sessions of treatment as well as 1 and 3 months after the last session of treatment

Apply the scores of different aging domains in VISIA system for evaluating the therapeutic response.

(minimum: 1, worse; maximum: 100, severe)

before the 1st, 2nd and 3rd sessions of treatment as well as 1 and 3 months after the last session of treatment
The scores of texture in VISIA system
Time Frame: before the 1st, 2nd and 3rd sessions of treatment as well as 1 and 3 months after the last session of treatment

Apply the scores of different aging domains in VISIA system for evaluating the therapeutic response.

(minimum: 1, worse; maximum: 100, severe)

before the 1st, 2nd and 3rd sessions of treatment as well as 1 and 3 months after the last session of treatment
The scores of pores size in VISIA system
Time Frame: before the 1st, 2nd and 3rd sessions of treatment as well as 1 and 3 months after the last session of treatment

Apply the scores of different aging domains in VISIA system for evaluating the therapeutic response.

(minimum: 1, worse; maximum: 100, severe)

before the 1st, 2nd and 3rd sessions of treatment as well as 1 and 3 months after the last session of treatment
The scores of pigment spots in VISIA system
Time Frame: before the 1st, 2nd and 3rd sessions of treatment as well as 1 and 3 months after the last session of treatment

Apply the scores of different aging domains in VISIA system for evaluating the therapeutic response.

(minimum: 1, worse; maximum: 100, severe)

before the 1st, 2nd and 3rd sessions of treatment as well as 1 and 3 months after the last session of treatment
The scores of brownish spots in VISIA system
Time Frame: before the 1st, 2nd and 3rd sessions of treatment as well as 1 and 3 months after the last session of treatment

Apply the scores of different aging domains in VISIA system for evaluating the therapeutic response.

(minimum: 1, worse; maximum: 100, severe)

before the 1st, 2nd and 3rd sessions of treatment as well as 1 and 3 months after the last session of treatment

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Yau-Li Huang, MD, Chang Gung Memorial Hospital, Taipei, Taiwan

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Anticipated)

November 30, 2021

Primary Completion (Anticipated)

August 31, 2022

Study Completion (Anticipated)

August 31, 2022

Study Registration Dates

First Submitted

October 1, 2021

First Submitted That Met QC Criteria

October 24, 2021

First Posted (Actual)

October 27, 2021

Study Record Updates

Last Update Posted (Actual)

October 27, 2021

Last Update Submitted That Met QC Criteria

October 24, 2021

Last Verified

September 1, 2021

More Information

Terms related to this study

Other Study ID Numbers

  • CMRPG5K0121

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

IPD Plan Description

We will not share IPD due to the privacy of participants.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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