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Effectiveness and Safety of Platelet-Rich Plasma in Restoration of the Skin in Periorbital Areas, Frontal Hairline, and Eyebrows

Effectiveness and Safety of Platelet-Rich Plasma in Restoration of the Skin in Periorbital Areas, Frontal Hairline, and Eyebrows

Status
Unknown
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20230516004
Enrollment
15
Registered
2023-05-16
Start date
2023-04-25
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Androgenetic Alopecia at hairline with mild to moderate wrinkle at periorbital Leukocyte poor Platelet-rich plasma, Restoration of the Skin in Periorbital Areas, Frontal Hairline, and Eyebrows

Interventions

Patients were treated with Platelet-rich plasma 3 sessions every 4 weeks. Then they were instructed to follow up at 1 month, 3 months, 6 months after the last treatments.
Experimental Device
Platelet-Rich Plasma

Sponsors

ASTRACO MEDICAL NETWORKS LTD.
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Aged 35-65 years 2. Both men and women 3. Mild to advanced photoaging by Glogau classification group I-III 4. Androgenetic Alopecia by dermoscopic criteria

Exclusion criteria

Exclusion criteria: 1. Pregnancy or lactation 2. Participants with using cream that affect wrinkle or colors or with antioxidant ingredients within 1 month before joining research 3. Participants with treatment like laser, filler or botulinum toxin injection within 3 month before joining research 4. Participants with history of low platelet or coagulopathy or taking medicine that interfere the coagulation like warfarin 5. Participants with needle phobia 6. Participants with history of allergy to anesthesia drug or sodium citrate 7. Participants with underlying disease of connective tissue diseases, autoimmune disease, immunosuppressive host or kelod 8. Participants with any psychological problem

Design outcomes

Primary

MeasureTime frame
Physician improvement scale Baseline, 4 weeks, 8 weeks, 12 weeks, 24 weeks, 36 weeks Physician global aesthetic improvement scale

Secondary

MeasureTime frame
Patient improvement scale Baseline, 4 weeks, 8 weeks, 12 weeks, 24 weeks, 36 weeks Physician global aesthetic improvement scale,Skin Texture Baseline, 4 weeks, 8 weeks, 12 weeks, 24 weeks, 36 weeks Antera,Skin Wrinkle Baseline, 4 weeks, 8 weeks, 12 weeks, 24 weeks, 36 weeks Antera,Skin elasticity Baseline, 4 weeks, 8 weeks, 12 weeks, 24 weeks, 36 weeks Cutometer,Melanin and Erythema Index Baseline, 4 weeks, 8 weeks, 12 weeks, 24 weeks, 36 weeks Mexameter,Physician global improvement at eyebrow Baseline, 4 weeks, 8 weeks, 12 weeks, 24 weeks, 36 weeks 7-Point grading scale,Physician global improvement at periorbital Baseline, 4 weeks, 8 weeks, 12 weeks, 24 weeks, 36 weeks 7-Point grading scale,Target area hair count baseline, 24 weeks, 36 weeks Trichoscan

Countries

Thailand

Contacts

Public ContactSasima Eimpunth

Faculty of Medicine Siriraj Hospital, Mahidol University

doctorsasima@gmail.com66858303555

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026