Clinical Trials Directory

Trials / Completed

CompletedNCT06562023

Botulinum Toxin and Mesotherapy on Enhancement of Facial Scarring

Botulinum Toxin Versus Mesotherapy on Enhancement of Facial Scarring (A Randomized Controlled Clinical Trial)

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
33 (actual)
Sponsor
Hams Hamed Abdelrahman · Academic / Other
Sex
All
Age
20 Years – 40 Years
Healthy volunteers
Not accepted

Summary

Most of the body's tissues can undergo wound repair following a disruption of tissue integrity. Upon healing, these wounds result in scar formation. The scars widen when the overlying musculature pulls apart suture lines. Botulinum Toxin A (BTA) is known to prevent fibroblast proliferation and it also induces temporary muscle paralysis. Also, mesotherapy is the non-invasive transdermal injection which can aid the skin to increase collagen and elastin production. Thus, both techniques are eligible for enhancement of facial scars.

Conditions

Interventions

TypeNameDescription
OTHERBotulinum Toxin Type APatients will receive BTA injection within a period of 5 days after primary closure.
OTHERMesotherapyPatients will receive mesotherapy growth factor serum with a derma pen within a period of 5 days after primary closure.

Timeline

Start date
2022-11-19
Primary completion
2024-07-20
Completion
2024-07-20
First posted
2024-08-20
Last updated
2024-08-20

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT06562023. Inclusion in this directory is not an endorsement.