Skip to content

Injection of Combination of 5-Fluorouracil and Triamcinolone versus Triamcinolone alone in Keloids

Comparative Study of Effectiveness of Combination of Intralesional 5-FU and Triamcinolone versus Triamcinolone alone in the Treatment of Keloids

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/06/034079
Enrollment
30
Registered
2021-06-08
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: L918- Other hypertrophic disorders of the skin

Interventions

Intervention1: Intralesional injection of combination of 5-Fluorouracil (5-FU) and Triamcinolone acetonide (TAC): Group A will receive intralesional TAC + 5-FU in the ratio of 1:9, prepared by taking
1: Mild itch
2: Moderate itch
3: Severe itch, (4) POSAS score (5) Adverse effects: ulceration, telangiectasia, skin atrophy, pigmentary changes etc. Control Intervention1: Intralesional injection of Triamcinolone acetonide (TAC) a

Sponsors

Lok Nayak Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: -All patients between 18-60 years, having keloid scars with maximum scar size of 20 cm2. -If one patient has multiple scars, no more than two scar sites will be included in the study.

Exclusion criteria

Exclusion criteria: -Pregnancy and lactation -Patients with co-morbidities like uncontrolled diabetes, hypertension, cardio-pulmonary disease, chronic liver / kidney disease with deranged LFT/KFT. -Any patient with history of treatment with intralesional TAC and /or 5-FU injection in previous 6 months for the same site. -Infected keloids

Design outcomes

Primary

MeasureTime frame
Clinical scar assessment by Vancouver Scar Scale (VSS) parameters of scar height, pliability, vascularity & pigmentation.Timepoint: Before 1st session (pre-drug), at every session and till last follow up at monthly intervals for subsequent 2 months after the last session.

Secondary

MeasureTime frame
Pain, Pruritis, Telangiectasia, Ulceration, Infection, Atrophy, Pigmentary changes, POSAS score, any other.Timepoint: Before 1st session (pre-drug), at every session and till last follow up at monthly intervals for subsequent 2 months after the last session.

Countries

India

Contacts

Public ContactDr Priyadarshini CA

Lok Nayak Hospital and associated Maulana Azad Medical College

drpsacademics@gmail.com09873617581

Outcome results

None listed

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