Subcision in Patients with Acnr Scar

Comparing the Effectiveness of Subcision using the classic method with Subcision using Endolift device in Patients with Acne scars

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20240920063099N1

Enrollment

Registered

2024-10-19

Start date

2024-12-21

Completion date

Unknown

Last updated

2025-01-08

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 group: Endolift laser subcision.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: The presence of Facial Acne Scars

Exclusion criteria

Exclusion criteria: Absence of Coagulation Diseases Use of Anticoagulant Drugs

Design outcomes

Primary

Measure	Time frame
Severity of Acne Scars. Timepoint: Examining the severity of Acne Scars at the beginning of the study and 30 days after subcision. Method of measurement: Photo and questionnaire.	—

Secondary

Measure	Time frame
Satisfaction score with your appearance. Timepoint: At the beginning of the study and 30 days after subcision. Method of measurement: The opinion of the patient (questionnaire).	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactTahere Khasti

Tehran University of Medical Sciences

khastitahere@gmail.com+98 901 742 2334

Outcome results

None listed

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