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The Effect of Platelet-rich Fibrin Matrix on Skin Rejuvenation

Not Applicable
Completed
Conditions
Skin Rejuvenation
Wrinkle
Nasolabial Fold
Skin Quality
Interventions
Procedure: PRFM injection
Procedure: Saline injection
Registration Number
NCT04128046
Lead Sponsor
New York Medical College
Brief Summary

Platelet-rich fibrin matrix (PRFM) is made from platelets that are extracted from a patient's blood, and many plastic surgeons and dermatologists have used it to fill in wrinkles and lines on the face. Both patients and doctors have observed that it gives extra volume in these areas and improves overall appearance. However, there is no research that shows how PRFM affects skin quality, such as pores, spots, red areas, and texture. The aim of this study is to determine whether PRFM has a role in rejuvenating facial skin.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
30
Inclusion Criteria
  • Adults 18 years of age and older who had a dermatological concern, specifically, conspicuous spots, pores, rhytids, uneven texture, or red or brown discoloration, and a VISIA complexion analysis score greater than 10
  • Agreed to continue any contraceptive hormonal therapy for duration of the study
  • Agreed to not initiate the use of hormonal therapy during the study
  • Agreed to not undergo any facial procedures or treatments, including injections and fillers, lasers, peels, and topical therapies, during the duration of the study
  • Agreed to adhere to a standardized skin care regimen throughout the duration of the study consisting of the use of a single cleanser and moisturizer twice a day
  • Agreed to refrain from excessive sun exposure/tanning
Exclusion Criteria
  • History of skin/connective tissue disorders
  • History of immunosuppressive therapy or radiotherapy
  • Participation in facial procedures, such as injections, lasers, peels, and dermabrasion, in the last six months
  • Use of topical/prescription acne medications in the last three months
  • Current smokers or prior smokers who quit fewer than 10 years ago

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
PRFMPRFM injectionHemi-face injected with PRFM. PRFM was produced from 9 mL of blood (Healeon Medical, Inc).
SalineSaline injectionHemi-face injected with saline.
Primary Outcome Measures
NameTimeMethod
Change in VISIA skin scoreSkin analysis performed at initial visit, at 6 weeks, and at 12 weeks following initial treatment

Difference between pre- and post-treatment VISIA analysis scores for skin parameters of spots, wrinkles, texture, and pores

Secondary Outcome Measures
NameTimeMethod
Change in Wrinkle Severity Rating ScaleRating occurred at initial visit, at 6 weeks, and at 12 weeks following initial treatment

Difference between pre- and post-treatment quantitative grading of nasolabial folds for each group. Graded from 1 through 5, with 5 representing the worst score

Skin Rejuvenation Outcomes Evaluation (SROE)Evaluation distributed at initial visit, at 6 weeks, and at 12 weeks following treatment.

Patient-reported outcome measure validated for skin resurfacing techniques. Each item is rated on a 0-4 scale. The final score is computed by dividing the total score for the instrument by 24 and multiplying by 100, giving a range of 0-100. The difference in the change in SROE score for each cohort was calculated.

VISIA Outcomes QuestionnaireEvaluation distributed at initial visit, at 6 weeks, and at 12 weeks following treatment.

Evaluation targeted specifically at identifying changes in the skin parameters analyzed by VISIA. Each item is rated on a 0-4 scale. The final score is computed by dividing the total score for the instrument by 24 and multiplying by 100, giving a range of 0-100. The difference in the change in VISIA outcomes score for each cohort was calculated.

Trial Locations

Locations (1)

New York Medical College

🇺🇸

Valhalla, New York, United States

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