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Investigating body striae treatment using endolift method and conditioning medium derived from fibroblast cells compared to microneedling method and conditioning medium derived from fibroblast cells

Evaluating the safety and efficacy of body striae treatment using the endolift method in combination with the conditioned medium derived from fibroblast cells foreskin compared to the microneedling method in combination with the conditioned medium derived from fibroblast cells: a randomized, blinded clinical trial study

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200127046282N37
Enrollment
20
Registered
2024-06-02
Start date
2024-06-09
Completion date
Unknown
Last updated
2024-06-24

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

Conditions

striae distensae. Atrophic disorder of skin, unspecified

Interventions

Intervention 1: Intervention group: In this group, patients are treated with endolift method along with 2 cc condition medium for three sessions with an interval of one month. Intervention 2: Control

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: Diagnosis of striae distensae based on the diagnosis of a dermatologist Patient satisfaction with the study Age less than 60 years and more than 20 years

Exclusion criteria

Exclusion criteria: Use any treatment to eliminate striae in the last three months Existence of skin lesions and diseases such as skin cancer wart Skin infection

Design outcomes

Primary

MeasureTime frame
Striae size. Timepoint: Before and 3 months after the intervention. Method of measurement: biometry.

Secondary

MeasureTime frame
Patient Satisfaction. Timepoint: Three months after treatment. Method of measurement: Questionnaire (It will be graded from 1 to 10).;Pain. Timepoint: Injection time. Method of measurement: questionnaire (It will be graded from 1 to 10).;Inflammation. Timepoint: 1-5 hours after injection. Method of measurement: Visit.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSona Zare

Skin and Stem Cell Research Center of Tehran University of Medical Sciences

sonazarebio@gmail.com+98 21 2665 7438

Outcome results

None listed

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