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Cannula-based Versus Needle-based Subcision for Posttraumatic Atrophic Facial Scars

Cannula-based Versus Common Needle-based Subcision in the Treatment of Posttraumatic Atrophic Facial Scars: A Clinical Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05747898
Enrollment
50
Registered
2023-02-28
Start date
2021-11-01
Completion date
2022-12-31
Last updated
2023-02-28

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

Conditions

Scar; Atrophy

Brief summary

This study aims to evaluate the effectiveness of cannula- based subcision versus common needle subcision in treatment of posttraumatic atrophic facial scars

Detailed description

In addition to cosmetic issues, atrophic scars can lead to psychological issues like social isolation, low self-esteem, and embarrassment. Subcision (Subcutaneous incision-less surgery) has been used for years to treat a variety of skin depressions, including atrophic acne scars and other depressed scars. Numerous modifications have been made throughout time to this surgical method to make it easier and more efficient. Although needle subcision is a straightforward, simple, useful, and practical procedure, it has many side effects and the overall success in this procedure is mild to moderate. So, in this study we evaluated the effectiveness of cannula- based subcision versus common needle subcision in treatment of posttraumatic atrophic facial scars.

Interventions

PROCEDUREcannula- based subcision

Insertion of a needle into the base of a cutaneous scar to cut fibrous tissue and help new collagen formation.

PROCEDUREcommon- needle based subcision

Insertion of a cannula into the base of a cutaneous scar to cut fibrous tissue and help new collagen formation.

Sponsors

Sohag University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Masking description

The assessor was blinded to the treatment applied to each half of the scar.

Intervention model description

Each scar was split into two equal halves; the upper right half were treated using a cannula- based subcision approach, while the lower left half was treated using a common needle-based procedure

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adult Patients (\> 20-years old) with posttraumatic facial scar

Exclusion criteria

* other types of scars (e.g; postacne scars), pregnancy, lactation, bleeding or coagulation disorders, liability for keloid formation, history of kobnerization, and patients with systemic diseases (cardiac, chronic renal diseases, chronic liver diseases, asthma and hypertension) at the time of recruitment.

Design outcomes

Primary

MeasureTime frameDescription
Vancouver scar scale (VSS)4 monthsThe (VSS) examines vascularity, pliability, pigmentation, and height, yielding a total score that ranges from 0 to 14. The original rating system was as follows: Vascularity (0=normal, 1=pink, 2=red, 3=purple), Pliability (Normal=0, Flat=0, Supple=1, Yielding=2, Firm=3, Ropes=4, Contracture=5), Pigmentation (0=normal, 1=hypo-pigmentation, 2=mixed pigmentation, 3=hyper-pigmentation), and Height (Flat=0 \<2 mm=1 2-5 mm=2 \>5 mm=2) .

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026