Skip to content

A COMPARATIVE STUDY ON EFFICACY AND SAFETY OF INTRALESIONAL INSULIN VS INTRALESIONAL TRIAMCINOLNE ACETONIDE VS INTRALESIONAL TRIAMCINOLONE ACETONIDE + 5-FLUOROURACIL FOR KELOID.

A PROSPECTIVE, COMPARATIVE, RANDOMIZED STUDY ON EFFICACY AND SAFETY OF INTRALESIONAL INSULIN VS INTRALESIONAL TRIAMCINOLNE ACETONIDE VS INTRALESIONAL TRIAMCINOLONE ACETONIDE + 5-FLUOROURACIL FOR KELOID. - NIL

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/11/097927
Enrollment
66
Registered
2025-11-24
Start date
Unknown
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

Health Condition 1: L910- Hypertrophic scar

Interventions

Intervention1: Intralesional Injection Insulin: Patients will be given intralesional short acting insulin at a dose of 10 IU/cm3 at an interval of 4 weeks for 4 months Control Intervention1: Intralesi

Sponsors

Dr.Jashanpreet Kaur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age 18 to 60 years Both male and female Clinical diagnosis of keloid equal to more than 3 months duration Keloid of size between 1 to 10 cubic centimeters. Willing to provide informed consent and comply with follow-up

Exclusion criteria

Exclusion criteria: -Age less than 18 or more than 60 years -Keloid of size more than 10 cubic centimeters. -Diabetic patients -Individuals receiving insulin or oral hypoglycemic drugs -Pregnant or lactating female -Immunocompromised patients -Patients on immunosuppressive drugs or systemic corticosteroids within last 3 months -Patients with evidence of bone marrow suppression including leukopenia,thrombocytopenia or anemia -Active infection or ulceration over lesion -Recent keloid treatment within last 8 weeks -Keloids on mucosa, eyelids or sites unsafe for injection -Coagulopathy or bleeding disorder -Hypersensitivity to study drugs -Individuals unwilling or unable to comply with the follow up schedule

Design outcomes

Primary

MeasureTime frame
To assess the clinical efficacy of Intralesional Insulin vs Intralesional Triamcinolone acetonide vs Intralesional Triamcinolone acetonide + 5-Fluorouracil in management of keloid.Timepoint: Baseline, 4, 8, 12 and 16 weeks

Secondary

MeasureTime frame
To study safety and tolerability of Intralesional Insulin vs Intralesional Triamcinolone Acetonide vs Intralesional Triamcinolone Acetonide + 5- Fluorouracil in management of keloid. Timepoint: 7 months

Countries

India

Contacts

Public ContactDr Jashanpreet Kaur

Shri Bhausaheb Hire Government Medical College

drchetanrajput@yahoo.com8888487808

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Sep 19, 2026