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Comparative study of topical TCA %50 and cultured autologous fibroblasts in the treatment of the atrophic scars of face.(Pilot Study)

Comparative study of topical TCA %50 and cultured autologous fibroblasts in the treatment of the atrophic scars of face. (Pilot Study)

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
IRCT
Registry ID
IRCT138902081159N2
Enrollment
20
Registered
2010-10-16
Start date
2010-05-22
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

atrophic scar. Scar conditions and fibrosis of skin

Interventions

Intervention 1: TCA 50%, topical, once monthly for 3 months. Intervention 2: Autologous fibroblasts (20million/mL), three times with 1-2 weeks intervals.
Treatment - Drugs
TCA 50%, topical, once monthly for 3 months.
Autologous fibroblasts (20million/mL), three times with 1-2 weeks intervals

Sponsors

Isfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Age more than 18 years, dissatisfaction of facial appearance, Negative pregnancy test at the screening visit, signing written informed consent, compliance with the study requirements, Healthy, non-scarred skin for biopsy Exclusion Criteria: Previous treatment with dermal filler or other method, participating in another clinical trial, History of autoimmune disease or organ transplantation, History of cancer, Active systemic infection, need to chronic antibiotic or steroidal therapy, Using systemic agents that increase bleeding or clotting, any disorder that increase bleeding or clotting, Pregnancy or breast feeding, Known allergic reaction to components of study treatment and/or study injection procedure, Excessive exposure to sun or sunburn in the post-auricular area, Patients with psychological disorders

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Scar size. Timepoint: before and after the intervention. Method of measurement: Photography of scar before beginning of the study and millimeter paper.

Secondary

MeasureTime frame
Cinical improvement of scar. Timepoint: Before the study and 3, 6, and 12 months after the beginning of study. Method of measurement: Photography of scar at each visit.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Mohamad Ali Nilforushzade

Skin Disease and Leishmaniasis Research Center (Sedigheh Tahereh)

Sdlrc@mui.ac.ir+98 31 1337 7767

Outcome results

None listed

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