Skip to content

Plasma Pen in the treatment of keloid scars

Effectiveness of Plasma Pen in the treatment of keloid scars

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220512054827N1
Enrollment
30
Registered
2022-07-20
Start date
2020-04-08
Completion date
Unknown
Last updated
2022-08-29

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

Conditions

Keloid Scars. Hypertrophic scar

Interventions

In each treatment session,the scar anesthetized with lidocaine gel then the keloids are removed by spot by spot method using plasma plexr device model plus.scars with a height of 2mm and less have bee

Sponsors

Islamic Azad University of Tehran Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 18 to 70 years old patients with keloid scars Volunteers who participated with informed consent Patients who have Possibility for repeated visits and follow-ups People with keloid scars with a maximum height of 5mm..

Exclusion criteria

Exclusion criteria: Patients who have history of previous treatments in the last six months Patients who have any chronic medical conditions that affects wound healing. People with underlying skin condition whose disease is exacerbated by skin irritations.

Design outcomes

Primary

MeasureTime frame
Keloid scar improvement. Timepoint: Before treatment and 5month after end of treatment. Method of measurement: Physical examination and scoring based on the Modified Vancouver Scar Scale.

Secondary

MeasureTime frame
Patient's satisfaction. Timepoint: 5 months after end of treatment. Method of measurement: Answer the patient by choosing one of the option:1)not changed 2) good 3)very good 4)excellent.;Postinflammatory hyperpigmentation (PIH)as Side effects of treatment. Timepoint: 10 days, one month and 5 months after the intervention. Method of measurement: Physical examination.;Recurrence. Timepoint: 10 days, one month and 3 month and 5 months after the intervention. Method of measurement: Physical examination and scoring based on the Modified Vancouver Scar Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSepideh Tehrani

Islamic Azad University of Tehran Medical Sciences

Stehrani@iautmu.ac.ir+98 21 2200 6660

Outcome results

None listed

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