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The efficacy and safety of fractional microneedle radiofrequency combined with autologous platelet rich plasma injection in the treatment of melasma: a prospective, single center, randomized half face controlled clinical study

The efficacy and safety of fractional microneedle radiofrequency combined with autologous platelet rich plasma injection in the treatment of melasma: a prospective, single center, randomized half face controlled clinical study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400080421
Enrollment
Unknown
Registered
2024-01-29
Start date
2024-02-15
Completion date
Unknown
Last updated
2024-02-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

melasma

Interventions

Experimental group:fractional microneedle radiofrequency therapy combined with autologous platelet rich plasma injection
Control group:fractional microneedle radiofrequency therapy combined with saline

Sponsors

Dermatology Department of the First Affiliated Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Stable stage chloasma (non inflammatory erythema period); 2. Patients aged 18-60; 3. Agree to follow the experimental treatment plan and visit plan, voluntarily enroll, and sign an informed consent form in writing.

Exclusion criteria

Exclusion criteria: 1. Any uncontrollable serious or potentially affecting clinical system disease history/surgical history for treatment and effectiveness evaluation, such as circulatory system, nervous system, hematological system, immune system, mental system diseases, etc; 2. During the treatment period, receive other facial rejuvenation treatments; 3. Exposure to sunlight without protective measures during treatment; 4. Have a history of malignant tumors; 5. Have undergone major surgery within the first 3 months of screening, or plan to undergo major surgery during the trial period; 6. Individuals who have participated or are currently participating in clinical trials of other intervention drugs or medical devices within the first 3 months of screening; 7. Screening for drugs that affect the condition of melasma or have photosensitive properties, such as other phototherapy, oral methotrexate, glutathione, oral contraceptives, isotretinoic acid, minocycline, etc., received within the first three months of screening; 8. The researcher believes that the subject has other situations that may affect compliance or be unsuitable for participation in this study; 9. Individuals with a history of drug abuse, drug use, or alcohol dependence before screening.

Design outcomes

Primary

MeasureTime frame
modified melasma area and severity index;VISIA image analysis system;Physician's global assessment, PGA;

Secondary

MeasureTime frame
Subject self-evaluation;

Countries

China

Contacts

Public ContactChen Jin

Dermatology Department of the First Affiliated Hospital of Chongqing Medical University

chenjin7791@163.com+86 185 2312 3177

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026