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Efficacy of microneedle radiofrequency with or without subcision for treatment of depressed acne scar

Comparison of the efficacy of microneedle radiofrequency combined with subcision vs microneedle radiofrequency alone in treatment of depressed acne scar

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016103130597N1
Enrollment
25
Registered
2017-01-26
Start date
2015-11-06
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

acne scar. Scar conditions and fibrosis of skin

Interventions

Intervention 1: Intervention group: in one side of the face, subcision was done and after 2 weeks, the process of treatment was followed by three sessions of microneedle radiofrequency. There was a 4-
Treatment - Devices
Intervention group: in one side of the face, subcision was done and after 2 weeks, the process of treatment was followed by three sessions of microneedle radiofrequency. There was a 4-week interval be
Control group: the other side of the face received microneedle radiofrequency without subcision during three sessions. There was a 4-week interval between each two sessions.

Sponsors

Vice Chancellor for research of Isfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion criteria: Age = 18 year; patient suffering from polymorphic and mixed acne; the acne scars should be in both sides of the face; Fitzpatrick skin types 2 to 4; informed consent for participation in the study. Exclusion Criteria: patients who are suffering from hypertrophic or Keloid scars.

Exclusion criteria

Exclusion criteria:

Design outcomes

Secondary

MeasureTime frame
Edema; Erythema; Pruritis; Hypo and Hyper pigmentation. Timepoint: After two weeks of each therapy session. Method of measurement: Patient self administered checklist of overall satisfaction.;Clinical improvement of atrophic scar. Timepoint: Baseline,three months after the last therapy session. Method of measurement: Serial photography and evaluation by two dermatologists blinded to the randomization process.;Patients satisfaction. Timepoint: Three months after the last therapy session. Method of measurement: Patient self administered checklist of overall satisfaction.

Primary

MeasureTime frame
Atrophic scar of acne. Timepoint: Baseline,three months after the last therapy session. Method of measurement: Serial photography and evaluation by two dermatologists blinded to the randomization process.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Nazila Poostiyan

Skin disease and Leishmaniasis Research Center, Isfahan University of Medical Sciences,

n.poostiyan@resident.mui.ac.ir+98 31 3668 5555

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 27, 2026