Clinical Trials Directory

Trials / Completed

CompletedNCT07034482

Efficacy and Safety of Intralesional 5-Fluorouracil and Triamcinolone Acetonide in Keloids and Hypertrophic Scars

Efficacy and Safety of Combination Therapy of Intralesional 5-Fluorouracil and Triamcinolone Acetonide in Treatment of Keloids and Hypertrophic Scars: A Prospective Study

Status
Completed
Phase
Study type
Observational
Enrollment
41 (actual)
Sponsor
Maharajgunj Medical Campus · Academic / Other
Sex
All
Age
16 Years
Healthy volunteers
Not accepted

Summary

Pathological scars like keloids and hypertrophic scars (HTS's) cause significant aesthetic, symptomatic and psychological issues to patients. Treatment is challenging with no universally accepted "gold standard" method. Plethora of options is in practice: intralesional (IL) injections, silicon sheets, lasers, cryotherapy, radiotherapy and surgery. This study analysed the effect of combination therapy of IL 5-fluorouracil (5-FU) and triamcinolone acetonide (TAC) in keloids and HTS's.

Conditions

Interventions

TypeNameDescription
DRUGIntralesional Triamcinolone 5 mg/mlSolution containing 5 mg TAC was injected intralesionally, every week for 6 weeks or until the scar flattened, whichever occurred earlier. Not more than 2 ml of the solution was injected per session, using 27G needle pre-mounted on an insulin syringe.
DRUGIntralesional 5-fluorouracilSolution containing 45 mg 5-FU was injected intralesionally, every week for 6 weeks or until the scar flattened, whichever occurred earlier. Not more than 2 ml of the solution was injected per session, using 27G needle pre-mounted on an insulin syringe.

Timeline

Start date
2020-09-01
Primary completion
2021-09-01
Completion
2021-09-01
First posted
2025-06-24
Last updated
2025-06-24

Locations

1 site across 1 country: Nepal

Source: ClinicalTrials.gov record NCT07034482. Inclusion in this directory is not an endorsement.