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Comparison of efficacy and safety of intralesional, triamcinolone hyaluronidase and combination of triamcinolone with hyaluronidase in the treatment of hypertrophic scars and keloid

Comparison of efficacy and safety of intralesional triamcinolone, hyaluronidase, and combination of triamcinolone with hyaluronidase in the treatment of hypertrophic scars and keloid

Status
Unknown
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20241208002
Enrollment
69
Registered
2024-12-08
Start date
2024-06-18
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Patient with hypertrophic scars and keloid hypertrophic scars,keloid

Interventions

Intralesional triamcinolone acetonide 40 mg/ml Administered drug in the upper dermis until slight blanching.maximum drug is triamcinolone acetonide 40 mg ,4 weeks interval for 3 session ,Intralesiona
Intralesional triamcinolone acetonide,Intralesional triamcinolone acetonide with hyaluronidase ,Intralesional hyaluronidase

Sponsors

Institute Srinakharinwirot University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1.Patient diagnosed with Keloid and hypertrophic scar 2.Measuring more than 3 mm. In height 3.Able to follow up examination 4.Participate in the project voluntarily and sign the consent

Exclusion criteria

Exclusion criteria: 1.Presentation of Other dermatology disease e.g.skin infection, Dermatitis ,psoriasis 2.Patients with underlying disease include Diabetes mellitus,Hypertension,Active peptic ulcer,osteroporosis,glaucoma or adrenal insufficiency 3.Patients with Immunocompromised host or liver failure or kidney failure 4.Patients prone to adrenal insufficiency by screening quesionaire 5.History steroid drugs useage in the form of injection or topical drugs within 3 months before the start of the study. 6. keloids and hypertrophic scar were treated in different ways within 3 months prior to the start of the study 7.History of allergy to triamcinolone acetonide or hyaluronidase or the ingredients of the injection such as Benzyl alcohol, Polysorbate 80, Carmellose sodium 8.History of allergy to steroid drug 9.History of allergy to bee, wasp or hornet 10.Pregnancy or lactation

Design outcomes

Primary

MeasureTime frame
Vancouver scar score at 12 weeks after end of the intervention Vancouver scar score

Secondary

MeasureTime frame
Height at 12 weeks after end of the intervention vernier caliper,Erythema index at 12 weeks after end of the intervention Mexameter,melanin index at 12 weeks after end of the intervention Mexameter,Pliability at 12 weeks after end of the intervention cutometer ,Patient and doctor satisfaction at 12 weeks after end of the intervention Visual analog scale,Triamcinolone level at 12 weeks after end of the intervention Triamcinolone level,Morning cortisol level at 12 weeks after end of the intervention Morning cortisol level

Countries

Thailand

Contacts

Public Contactsalinee rojhirunsakool

Faculty of Medicine,Srinakharinwirot University

salinee.roj@gmail.com0894159665

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026