Skip to content

Evaluation of efficacy and safety skin of MPT non-crosslinked hyaluronic acid subdermal injection for facial Rejuvenation in Thai population

Evaluation of efficacy and safety skin of MPT non-crosslinked hyaluronic acid subdermal injection for facial Rejuvenation in Thai population

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20251127004
Enrollment
30
Registered
2025-11-27
Start date
2024-09-11
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

Patient with photoaging skin non-crosslinked hyaluronic acid, facial rejuvenation

Interventions

Patients were injected with MPT non-crosslinked hyaluronic acid for three sessions at one-month intervals. They were then instructed to follow up at 1, 2, 3, 6, and 9 months after the final treatment.
Experimental Device
MPT non-crosslinked hyaluronic acid

Sponsors

Faculty of Medicine Siriraj Hospital, Mahidol University, Thailand
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Male and female Thai volunteers aged between 20 - 60 years. 2. Individuals with early-stage photoaged skin, as assessed by at least one of the following criteria: 2.1. Uneven skin tone 2.2. Fine wrinkles 2.3. Dry skin 2.4. Skin laxity

Exclusion criteria

Exclusion criteria: 1. Pregnant or breastfeeding women. 2. Volunteers with a history of platelet disorders, coagulation abnormalities, anemia, liver disease, cancer, or autoimmune disorders. 3. Volunteers who smoke or have a history of heavy alcohol consumption. 4. Volunteers with dermatitis, wounds, or skin infections on the face. 5. Volunteers with a history of allergy to local anesthetics. 6. Volunteers who regularly take hormones, contraceptives (oral or injectable), or NSAIDs. 7. Volunteers taking anticoagulants or antiplatelet drugs such as aspirin. 8. Volunteers who have undergone facial tightening procedures (e.g., energy-based devices or thread lifting) within 6 months prior to participation. 9. Volunteers who have received filler injections on the face within 6 months prior to participation. 10. Volunteers who have undergone platelet-rich plasma (PRP) injections on the face within 6 months prior to participation. 11. Volunteers who have received botulinum toxin injections on the face within 6 months prior to participation. 12. Volunteers who have undergone collagen-stimulating laser treatments on the face (e.g., Picosecond laser, Er:YAG laser, Fractora, or E-matrix laser) within 6 months prior to participation. 13. Volunteers with a history of keloid formation. 14. Volunteers diagnosed with psychiatric disorders by a psychiatrist.

Design outcomes

Primary

MeasureTime frame
Wrinkle depth Baseline, 2nd treatment, 3rd treatment, 1, 2, 3, 6 and 9 months after 3rd treatment Antera,Hydration Baseline, 2nd treatment, 3rd treatment, 1, 2, 3, 6 and 9 months after 3rd treatment Corneometer,Wrinkle index Baseline, 2nd treatment, 3rd treatment, 1, 2, 3, 6 and 9 months after 3rd treatment Antera,Texture Baseline, 2nd treatment, 3rd treatment, 1, 2, 3, 6 and 9 months after 3rd treatment Antera

Secondary

MeasureTime frame
R0 parameter (indicate skin firmness) Baseline, 2nd treatment, 3rd treatment, 1, 2, 3, 6 and 9 months after 3rd treatment Cutometer,R2 parameter (indicate skin elasticity) Baseline, 2nd treatment, 3rd treatment, 1, 2, 3, 6 and 9 months after 3rd treatment Cutometer,Redness Baseline, 2nd treatment, 3rd treatment, 1, 2, 3, 6 and 9 months after 3rd treatment Mexameter,Pigmentation Baseline, 2nd treatment, 3rd treatment, 1, 2, 3, 6 and 9 months after 3rd treatment Mexameter,Sebum level Baseline, 2nd treatment, 3rd treatment, 1, 2, 3, 6 and 9 months after 3rd treatment Sebumeter,ITA value Baseline, 2nd treatment, 3rd treatment, 1, 2, 3, 6 and 9 months after 3rd treatment colorimeter,Volume change Baseline, 2nd treatment, 3rd treatment, 1, 2, 3, 6 and 9 months after 3rd treatment Vectra H2,Safety Baseline, 2nd treatment, 3rd treatment, 1, 2, 3, 6 and 9 months after 3rd treatment Adverse event,Physician improvement scale Baseline, 2nd treatment, 3rd treatment, 1, 2, 3, 6 and 9 months after 3rd treatment percent improvement, Patient Improvement scale Baseline, 2nd treatment, 3rd treatment, 1, 2, 3, 6 and 9 months after 3rd treatment percent improvement,Pain score Baseline, 2nd treatment, 3rd treatment Visual analog scale

Countries

Thailand

Contacts

Public ContactRungsima Wanitphakdeedecha

Faculty of Medicine Siriraj Hospital, Mahidol University

rungsima.wan@mahidol.ac.th6624197000

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026