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To evaluate the safety and efficacy of M3D Fractional - Made By Medaria in reducing facial aging

To evaluate the safety and efficacy of M3D Fractional - Made By Medaria in reducing facial aging: A single arm phase III clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201507226135N5
Enrollment
15
Registered
2015-07-24
Start date
2015-07-23
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Facial aging.

Interventions

Each patient will receive six sessions of m3D Fractional treatment to the whole face. The face will be thoroughly cleaned and dried before treatment. Treatment will be conducted by trained and experie
Treatment - Devices

Sponsors

Medaria Company
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: • Aged between 30 to 60 years. • Mild to moderate (Glogaue Score) • Skin Type (II-IV) • Signed informed consent voluntarily and knowingly Exclusion criteria • History of any implant in face area • History of any cosmetic surgery during last 3 years in face area • History of RF during last year • History of any Botulinum, laser, or intense pulsed light during last 6 month • History of Isotretinoin during last 6 month • Collagen vascular disease • Diabetes • Severe cardiac disease • Malignant tumor • Bleeding disorders, Coagulopathy, any drugs affect bleeding time • Any active, chronic and recurrent infection • Any history of anaphylaxis • Susceptibility to keloids • Any active or recurrent herpes • Any immune-compromised conditions • Skin atrophy • Active smoker ( last 2 years) • Pregnancy/ breast feeding • Vascular disease • Cardiac pace maker • Vertigo, labyrinthitis • Dyslipidemia

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Wrinkle. Timepoint: At baseline- 1 week, 3 months and 6 months after the last treatment session. Method of measurement: Two board-certified dermatologists will perform clinical assessments in a blinded fashion by scoring every photograph according to the Fitzpatrick wrinkle scale.;Laxity. Timepoint: At baseline- 1 week, 3 months and 6 months after the last treatment session. Method of measurement: Two board-certified dermatologists will perform clinical assessments in a blinded fashion by scoring every photograph according to the Alexiades-Armenakas laxity scale.

Secondary

MeasureTime frame
Patient's overall satisfaction. Timepoint: At the final treatment session and at 1-week, 3- month and 6- month after their final treatment session. Method of measurement: based on a 6-point Likert scale (0-No satisfaction, 1- very little satisfaction, 2-little satisfaction, 3-moderate satisfaction, 4-much satisfaction, 5- very much satisfaction).;Skin elasticity. Timepoint: At baseline and 1-week, 3- month and 6-month after the final treatment session. Method of measurement: Cutometer.;Water content. Timepoint: At baseline and 1-week, 3- month and 6-month after the final treatment session. Method of measurement: Corneometer.;Transepidermal water loss. Timepoint: At baseline and 1-week, 3- month and 6-month after the final treatment session. Method of measurement: TEWAmeter.;Skin pigmentation. Timepoint: At baseline and 1-week, 3- month and 6-month after the final treatment session. Method of measurement: Mexameter.;Ultrasonographic measurements ( skin thickness and density). Timepoint: At baseline and 1-week, 3- month and 6-month after the final treatment session. Method of measurement: Skin ultrasonography.;Wrinkles and colour differences. Timepoint: At baseline and 1-week, 3- month and 6-month after the final treatment session. Method of measurement: VisioFace.;Side-effects including erythema, edema, pain, hyperpigmentation and scarring). Timepoint: All visits. Method of measurement: By physician.

Countries

Iran (Islamic Republic of)

Outcome results

None listed

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